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1
94
(ATP) P. 7
(AP) P. 13
S1
330
131014004S1-01 21 13:1014:00
140014504S1-02 14:0014:50
150015504S1-03 15:0015:50
155016404S1-04 15:5016:40
S2
327
110012001S2-01 4711:0012:00
327 13001400
1S2-02 13:0014:00
143015301S2-03 14:3015:30
328
13401520
329
130014003S2-01 13:0014:00
143015303S2-02 14:3015:30
S3 1 121
327
133014301S3-01 13:3014:00
1S3-02 14:0014:30
143015301S3-03 QM/MM14:3015:00
1S3-04 15:0015:30
160017301S3-05 16:0016:30
1S3-06 --16:3017:00
1S3-07 17:0017:30
S4 1 131
327
133013351S4-01 13:3013:35
133515101S4-02 13:3514:10
1S4-03 14:1014:45
1S4-04 14:4515:10
152017051S4-05 15:2015:55
1S4-06 15:5516:30
1S4-07 16:3017:05
-
2
S5 1
- II
327
900 10201S5-01 09:0009:05
1S5-02 FIBER09:0509:30
1S5-03 JST 09:3009:55
1S5-04 RNA09:5510:20
102011201S5-05 10:2010:50
1S5-06 10:5011:20
112012301S5-07 11:2011:50
1S5-08 In Vivo JSTCREST11:5012:20
1S5-09 12:2012:30
2014
327
13301730
329
900 1210
329
13301730
330
133013554S5-01 13:3013:35
4S5-02 13:3513:55
135514454S5-03 Exciting New Enzymes From Fungal BiosyntheticPathwaysUin. of California, Los AngelesYI, Tang13:5514:25
4S5-04 14:2514:45
144515354S5-05 Semi-synthetic artemisinin: Using synthetic biologyto increase the supply of a crucial antimalarial drugAmyris, Inc.MICHAEL, Leavell14:4515:15
4S5-06 15:1515:35
153516154S5-07 15:3515:55
4S5-08 15:5516:15
S6 2
- 2014-
327
930 940 1S6-01 09:3009:40
940 10301S6-02 JASRI 09:4010:00
1S6-03 10010:0010:30
103011301S6-04 10:3011:00
1S6-05 11:0011:30
113012001S6-06 BiNiO3 11:3012:00
327
133015001S6-07 13:3013:40
1S6-08 13:4014:00
1S6-09 14:0014:20
1S6-10 14:2014:40
1S6-11 Pillar[n]arene14:4015:00
151016301S6-12 15:1015:30
1S6-13 ALCA, JST 15:3015:50
1S6-14 Photochemical Organocatalytic ReactionsICIQ,Institute of Chemical Research of Catalonia, SpainMELCHIORRE, Paolo15:5016:30
328
900 1110
The Chemical Record Lecture 2014
328
15301620
-
3
8
329
13301715
330
930 10304S6-01 09:3009:35
4S6-02 09:3510:00
4S6-03 10:0010:15
4S6-04 10:1510:30
104012304S6-05 10:4010:55
4S6-06 10:5511:10
4S6-07 11:1011:25
4S6-08 CREST11:3511:50
4S6-09 11:5012:05
4S6-10 12:0512:30
330
133013354S6-11 13:3013:35
133514004S6-12 13:3514:00
140014254S6-13 14:0014:25
142514504S6-14 14:2514:50
145015154S6-15 JST14:5015:15
151515404S6-16 15:1515:40
154016054S6-17 EL15:4016:05
160516304S6-18 OLED OPERA 16:0516:30
S7
JST
327
930 12101S7-01 Opnening RemarksTokyo Metoro. Univ.INOUE, Haruo09:3009:40
1S7-02 Activating solar energy fuctions in perovskite-type metal oxidesCALTECHYAMAZAKI, Yoshihiro09:4010:10
1S7-03 In situ characterization of photo energy conversion processes at solid/liquid interfacesNIMSNOGUCHI, Hidenori10:1010:40
1S7-04 Metal Binding by Organic Dyes under Chemical and PhotochemicalControlInst. Mol .Sci.MURAHASHI, Tetsuro10:4011:10
1S7-05 Development of Light-energy and Molecular Material ConversionCatalysts Constructed inside a Cage-type MoleculeOsaka Univ.FUNAHASHI, Yasuhiro11:1011:40
1S7-06 Creation of highly ecient water-splitting photocatalysts through thecontrol of surface band structureTokyo Inst.Tech.MAEDA, Kazuhiko11:4012:10
32713201800
1S7-07 Articial Photosynthesis Water Oxidation Is The KeyRoyal Institute of Tech. (KTH, SwedenSUN, Licheng13:2014:10
1S7-08 Development of highly ecient water oxidation catalysts usingpolyoxometalatesHiroshima Univ.SADAKAE, Masahiro14:1014:40
1S7-09 Optical Trapping and Photochemical Reactions/Energy Conversion ata Plasmonic Nano-AntennaOsaka City Univ.TSUBOI, Yasuyuki14:4015:10
1S7-10 Elucidation of regulatory mechanisms of photochemical reaction inphotosynthesis to create stable molecular devicesKyoto Univ.IFUKU,Kentaro15:2515:55
1S7-11 Elucidation of molecular mechanisms of highly ecient energyconversion and water oxidation by photosynthesis Ehime Univ.SUGIURA, Miwa15:5516:25
1S7-12 Articial metabolic processes powered by photosynthesisKanagawaUniv.NAGASHIMA, kenji V.P.16:2516:55
1S7-13 Multimodal spectral microscope for understanding chloroplast activityand overall cellular physiology in oil-producing algaeKyoto Univ.KUMAZAKI, Shigeichi16:5517:25
1S7-14 Super-resolution uorescence microscopy of biomineralization indiatomsYamagata Univ.HOTTA, Jun-ichi17:2517:55
1S7-15 Closing RemarksJST17:5518:00
328
133013402S7-01 13:3013:40
134015252S7-02 13:4014:15
2S7-03 14:1514:50
2S7-04 14:5015:25
153517202S7-05 15:3516:10
2S7-06 16:1016:45
2S7-07 --16:4517:20
-
4
S8 3
327
930 940 1S8-01 09:3009:40
940 10101S8-02 JST-ERATO 09:4010:10
101010401S8-03 10:1010:40
104011001S8-04 10:4011:00
111011301S8-05 palauamine11:1011:30
113012001S8-06 11:3012:00
120012301S8-07 ET743 12:0012:30
327
133014101S8-08 NIH 13:3013:35
1S8-09 13:3514:10
141014451S8-10 --14:1014:45
144515201S8-11 PET14:4515:20
152015551S8-12 15:2015:55
155516301S8-13 15:5516:25
1S8-14 16:2516:30
328
100010502S8-01 Visible light photoredox catalysis as key stepfor organic synthesisUniv. RegensburgOLIVER, Reiser10:0010:50
110011502S8-02 Photosynthetic membrane architecture investi-gated by mass spectrometric analysisWashington University in St. LouisBLANKENSHIP, Robert E.11:0011:50
328
133014452S8-03 5 CS3 13:3013:45
2S8-04 FLEC13:4514:15
2S8-05 !14:1514:45
144515452S8-06 (Mg,Li)14:4515:15
2S8-07 15:1515:45
154517152S8-08 CEMS15:4516:15
2S8-09 16:1516:45
2S8-10 16:4517:15
21
329
13301700
330
930 10354S8-01 09:3009:35
4S8-02 09:3509:55
4S8-03 -09:5510:15
4S8-04 WPI-ITbMJST-ERATO10:1510:35
103511254S8-05 G10:3510:50
4S8-06 WPI-ITbM10:5011:10
4S8-07 11:1011:25
112512154S8-08 11:2511:40
4S8-09 11:4011:55
4S8-10 11:5512:10
4S8-11 12:1012:15
330
133015104S8-12 13:3013:35
4S8-13 MANA 13:3514:10
4S8-14 14:1014:40
4S8-15 14:4015:10
-
5
152016304S8-16 15:2015:50
4S8-17 JST CREST15:5016:25
4S8-18 16:2516:30
S9 1
327
930 11151S9-01 09:3009:35
1S9-02 09:3510:00
1S9-03 10:0010:25
1S9-04 10:2510:50
1S9-05 10:5011:15
111512301S9-06 11:1511:40
1S9-07 JST11:4012:05
1S9-08 12:0512:25
1S9-09 JST12:2512:30
327
133014251S9-10 13:3013:35
1S9-11 13:3514:00
1S9-12 JST 14:0014:25
142515251S9-13 14:2514:55
1S9-14 14:5515:25
152516301S9-15 15:2515:55
1S9-16 LEDJST/ERATO 15:5516:25
1S9-17 JST 16:2516:30
328
133015202S9-01 13:3013:40
2S9-02 13:4014:05
2S9-03 JST CREST14:0514:30
2S9-04 14:3014:55
2S9-05 14:5515:20
152016452S9-06 15:2015:45
2S9-07 -JST-CREST15:4516:10
2S9-08 JST CREST16:1016:35
2S9-09 16:3516:45
329
13001700
X
330
930 12304S9-01 09:3009:35
4S9-02 X09:3510:05
4S9-03 X 10:0510:30
4S9-04 GISAXS10:3010:50
4S9-05 CREST10:5011:10
4S9-06 X11:1011:30
4S9-07 X 11:3011:50
4S9-08 X11:5012:10
4S9-09 X 12:1012:30
330
133014304S9-10 13:3013:50
4S9-11 13:5014:10
4S9-12 14:1014:30
143015304S9-13 14:3014:50
4S9-14 14:5015:10
4S9-15 15:1015:30
153016304S9-16 15:3015:50
4S9-17 15:5016:10
4S9-18 Ge=Ge[2]16:1016:30
-
6
SA 2
327
930 12301SA-01 09:3009:50
1SA-02 - 09:5010:20
1SA-03 10:2010:50
1SA-04 11:0011:30
1SA-05 11:3012:00
1SA-06 SiWPI-MANAJST12:0012:30
327
133014351SA-07 13:3013:35
1SA-08 13:3514:05
1SA-09 PET14:0514:35
143515351SA-10 14:3515:05
1SA-11 15:0515:35
153516051SA-12 iPS15:3516:05
160516351SA-13 16:0516:35
Reaxys Prize Club in Japan 2014
328
14001700
14 2
329
13151730
330
930 11104SA-01 1 2 309:3009:55
4SA-02
09:5510:204SA-03 10:2010:45
4SA-04 10:4511:10
111012304SA-05 Si""NTT 11:1011:35
4SA-06 11:3512:00
4SA-07 12:0012:25
4SA-08 12 : 2512:30
330
133014504SA-09 13:3013:50
4SA-10 13:5014:10
4SA-11 JST 14:1014:30
4SA-12 14:3014:50
151016304SA-13 Kim 15:1015:30
4SA-14 15:3015:50
4SA-15 1 15:5016:10
4SA-16 16:1016:30
SB S21
329
13301740
-
7
(ATP)
F4 S10
327
130013101F4-25 13:0013:10
131016501F4-26 13:1013:40
1F4-29 Unstructured/Structured Interaction13:4014:10
1F4-32 HGF14:1014:40
1F4-35 14:4015:001F4-37 15:0015:30
1F4-40 15:3016:00
1F4-43 Phoenix Venture Partners (PVP)16:0016:30
1F4-46 16:3016:50
328
920 11002F4-03 09:2009:30
2F4-04 (FCEV)09:3010:20
2F4-09 45 PEFC10:2010:50
2F4-12 10:5011:00
110012102F4-13 11:0011:40
2F4-17 PEFC 11:4012:10
328 13101520
2F4-26 13:1014:00
2F4-31 14:0014:40
2F4-35 I2CNER14:4015:10
2F4-38 15:1015:20
152017202F4-39 Bloom EnergyJapan15:2016:00
2F4-43 16:0016:40
2F4-47 16:4017:20
329
130013103F4-25 13:0013:10
131014503F4-26 13:1014:00
3F4-31 14:0014:40
3F4-35 14:4014:50
145016103F4-36 14:5015:30
3F4-40 JST-CREST15:3016:10
161017003F4-44 16:1016:40
3F4-47 16:4017:00
F5 S11
327
900 10401F5-01 WPI-AIMR09:0009:101F5-02 LIXIL09:1009:40
1F5-05 09:4010:10
1F5-08 VOIGT Dagmar10:1010:40
104012201F5-11 10:4011:10
1F5-14 11:1011:40
1F5-17 11:4012:20
327 12501410
1F5-24 12:5013:40
1F5-29 TRIZ 13:4014:10
141015401F5-32 14:1014:40
1F5-35 RGB14:4015:10
-
8
1F5-38 15:1015:40
154017201F5-41 15:4016:10
1F5-44 R&D 16:1016:40
1F5-47 16:4017:20
328
101010202F5-08 10:1010:20
102012002F5-09 10:2011:10
2F5-14 11:1011:202F5-15 GSC11:2012:00
328 13001410
2F5-25 13:0013:30
2F5-28 13:3014:00
2F5-31 14:0014:10
141015302F5-32 14:1014:50
2F5-36 14:5015:20
2F5-39 15:2015:30
153016002F5-40 ( )15:3016:00
160016102F5-43 16:0016:10
329
130013103F5-25 13:0013:10
131014203F5-26 PE PET 13:1013:50
3F5-30 GP13:5014:20
142015403F5-33 14:2014:50
3F5-36 14:5015:003F5-37 QMONOS15:0015:40
154017003F5-41 15:4016:10
3F5-44 PET16:1016:50
3F5-48 16:5017:00
G6 S20
327
133015301G6-28 13:3013:401G6-29 13:4014:30
1G6-34 14:3014:401G6-35 14:4015:20
1G6-39 15:2015:30
153017101G6-40 CNT 15:3016:10
1G6-44 16:1016:201G6-45 16:2017:00
1G6-49 17:0017:10
328
930 940 2G6-04 JX09:3009:40
940 12002G6-05 09:4010:30
2G6-10 10:3010:402G6-11 10:4011:20
2G6-15 11:2012:00
328 13001550
2G6-25 5-13:0013:40
2G6-29 13:4014:20
2G6-33 14:2014:302G6-34 ACT-C 14:3015:10
2G6-38 15:1015:50
329
920 12103G6-03 09:2009:303G6-04 09:3010:20
3G6-09 10:2010:30
-
9
3G6-10 JST/ACT-C10:3011:10
3G6-14 11:1011:203G6-15 11:2012:00
3G6-19 12:0012:10
329 13101450
3G6-26 I2CNER : Powering the Future, InternationalizingResearchI2CNER, Kyushu Univ.SOFRONIS, Petros13:1014:00
3G6-31 Incubation Time14:0014:103G6-32 14:1014:40
3G6-35 14:4014:50
150016403G6-37 15:0015:40
3G6-41 15:4015:503G6-42 Lignocellulose 15:5016:30
3G6-46 16:3016:40
G7 S21
327
122015001G7-21 12:2013:10
1G7-26 13:1013:40
1G7-29 - -13:4014:20
1G7-33 14:2014:50
1G7-36 14:5015:00
150017201G7-37 15:0015:40
1G7-41
15:4016:201G7-45 16:2016:50
1G7-48 16:5017:20
H5 S30
327
100010101H5-07 FLEC10:0010:10
101012101H5-08 10:1011:00
1H5-13 Li11:0011:40
1H5-17 11:4012:10
327 13101450
1H5-26 13:1013:50
1H5-30 FLEC 13:5014:20
1H5-33 JST/ERATO14:2014:50
151016501H5-38 Development of Taste Sensing SystemFac. Sci. Tech.,Keio Univ.CITTERIO, Daniel; SUZUKI, Koji15:1015:50
1H5-42 JSRJSR 15:5016:20
1H5-45 NVRAM16:2016:50
328 900 1200
2H5-01 09:0009:40
2H5-05 09:4010:10
2H5-09 10:2011:00
-
10
2H5-13 TFT 11:0011:30
2H5-16 EL11:3012:00
328
130013102H5-25 13:0013:10
131015102H5-26 13:1014:00
2H5-31 14:0014:30
2H5-34 iCeMS 14:3015:10
153017102H5-40 15:3016:10
2H5-44 16:1016:40
2H5-47 16:4017:10
329 920 1040
3H5-03 09:2010:00
3H5-07 10:0010:40
104012203H5-11 XJST10:4011:10
3H5-14 11:1011:50
3H5-18 11:5012:20
329 13301530
3H5-28 13:3014:20
3H5-33 14:2014:50
3H5-36 14:5015:30
155017303H5-42 15:5016:20
3H5-45 JST 16:2017:00
3H5-49 17:0017:30
330 10001230
4H5-07 CZTS 10:0010:40
4H5-11 CZTS 10:4011:10
4H5-14 11:1011:50
4H5-18 11:5012:30
P
32712301400
1PB-201
1PB-202
1PB-203 NEC
1PB-204 X ICP-MS CO2
1PB-205 CO2
1PB-206 (SqRAFTwP)
1PB-207 CO2
1PB-208
1PB-209
1PB-210
1PB-211
1PB-212 GaN LED
1PB-213
1PB-214
1PB-215
1PB-216
1PB-217 Cu Cu
1PB-218 D-A
1PB-219
1PB-220
1PB-221
1PB-222
-
11
1PB-223 FLEC
1PB-224 BNCT BNCT
1PB-225 BNCT
1PB-226 -1,3-
1PB-227 JVCJVC
1PB-228
1PB-229 in vivo
1PB-230 Rational design of spirocyclic rhodamine derivatives for multi-colorcancer imagingGrad. Sch. Med., The Univ. of Tokyo; Grad. Sch. Pharm.,The Univ. of Tokyo; JST Basic Research ProgramIWATATE, Ryu john;KAMIYA, Mako; URANO, Yasuteru
1PB-231
1PB-232 1-acetoxychavicol acetate (ACA)
1PB-233
1PB-234
1PB-235 IER5/Cdc25B
1PB-236 HasA
1PB-237
1PB-238 Design and synthesis of antimalarial agents with indoloquinolonecoresGrad. Sch. Nat. Sci. Technol., Okayama Univ.WANG, Ning; LU,Wen-jie; HAYASHI, Ikuya; KAWAFUCHI, Hiroyuki; INOKUCHI,
Tsutomu
1PB-239 Network structures in polysaccharide gels and its eect onswallowingGrad. Sch. Marine Sci. and Technol., Tokyo Univ. of MarineSci. and Technol.MATSUKAWA, Shingo; BRENNER, Tom; SHIMADA,Ryota
1PB-240
1PB-241
1PB-242
1PB-243 TIMP
32715001630
1PC-201 JST ,C R E S T MUCKERMAN James T.
1PC-202 SPS
1PC-203
1PC-204 CaMn2O4*xH2O
1PC-205
1PC-206
1PC-207
1PC-208 GaN-Si
1PC-209 CO2
1PC-210 Block Copolymer-Mediated Transfer Printing of Nanostructures:Application in Solar CellsAIST Renewable Energy Research CenterMIZUNO, Hidenori; SAI, Hitoshi; MATSUBARA, Koji; KONDO, Michio
1PC-211
1PC-212
1PC-213 JST
1PC-214
1PC-215 JST CREST
1PC-216
1PC-217 JST CREST
1PC-218 Cs
1PC-219
1PC-220
1PC-221
1PC-222 5cm
1PC-223 WANGWanhuiMUCKERMAN James T.
1PC-224 Y/N
1PC-225
1PC-226
1PC-227
1PC-228
GSC1PC-229
1PC-230
1PC-231
1PC-232
1PC-233
-
12
1PC-234 N-
1PC-235 /JST CRESTUYANIK Muhammet
1PC-236
1PC-237 --
1PC-238
1PC-239 Boronic Acid-DMAP(O) Cooperative Catalysis for DehydrativeCondensation between Carboxylic Acids and AminesGrad. Sch. Eng.,Nagoya Univ.LU, Yanhui; ISHIHARA, Kazuaki
1PC-240 -
1PC-241
1PC-242 Optical properties of confeito-like Au nanoparticles and theirapplicationsNational Univerisity of Science and TechnologyUJIHARA,Masaki; IMAE, Toyoko
1PC-243
1PC-244
1PC-245 PEG
1PC-246
1PC-247
1PC-248
1PC-249
1PC-250 P450BM3
1PC-251
1PC-252
1PC-253
1PC-254
1PC-255
1PC-256
1PC-257
-
13
(AP)
A1 7
F
327
950 1050 PC 9409501A1-06, 1A1-07, 1A1-08, 1A1-09,
1A1-10, 1A1-111A1-06 :WPI-ITbM
1A1-07 (1--2-)
1A1-08
1A1-09 C2
1A1-10 1-
1A1-11 (S)-trans-
11001200 PC 105011001A1-13, 1A1-14, 1A1-15, 1A1-16,
1A1-171A1-13 5,10-[5]
1A1-14 [33](1,3,5) Si-Si Aung
1A1-15 [2+2]
1A1-16 1,2-, 1,3- 2-
1A1-17* Synthesis and Photochemical Reactivity of Caged-compounds withNovel Stilbene-based Two-photon ChromophoreGrad. Sch. Sci., HiroshimaUniv.BOINAPALLY, Srikanth; ABE, Manabu
327 13101410
PC 130013101A1-26, 1A1-29, 1A1-301A1-26
1A1-29 2-
1A1-30*
14201520 PC 141014201A1-33, 1A1-34, 1A1-35, 1A1-36,
1A1-381A1-33 2,5--3,6--1,4-()
1A1-34
1A1-35
1A1-36* CC
1A1-38 2,6-
15301630 PC 152015301A1-40, 1A1-41, 1A1-42, 1A1-43,
1A1-44, 1A1-45
1A1-40 (9-)()
1A1-41 DNA ATS
1A1-42 DNA
1A1-43
1A1-44 -5 PEG-
1A1-45
16401730 PC 163016401A1-47, 1A1-48, 1A1-49, 1A1-50,
1A1-511A1-47
1A1-48
1A1-49
1A1-50
1A1-51 REMELLO SebastianNybin
328 950 1050
PC 9409502A1-06, 2A1-07, 2A1-08, 2A1-09,2A1-10
2A1-06
2A1-07
2A1-08 Kuttassery FazalurahmanMathew Siby
2A1-09 ALCA, JST
2A1-10* Re CO2XAFS
11001200 PC 105011002A1-13, 2A1-14, 2A1-15, 2A1-16,
2A1-17, 2A1-182A1-13
2A1-14
2A1-15 (III)
2A1-16
2A1-17 Viviani Vadim
2A1-18
328 13101410
PC 130013102A1-26, 2A1-27, 2A1-28, 2A1-29,
-
14
2A1-30, 2A1-312A1-26 1
2A1-27 2
2A1-28 -
2A1-29
2A1-30
2A1-31
A2 8
B
327
920 1010 PC 9109201A2-03, 1A2-04, 1A2-05, 1A2-06,
1A2-071A2-03
1A2-04
1A2-05 --
1A2-06
1A2-07
10201100 PC 101010201A2-09, 1A2-10, 1A2-11, 1A2-121A2-09 [2+2]
1A2-10 Regioselective synthesis of 1,4-bisfunctionalized fullerenes via NBS-promoted oxidation of fullerene monoradicalWPI-AIMR, Tohoku Univ.SI, Weili; ASAO, Naoki; YAMAMOTO, Yoshinori; JIN, Tienan
1A2-11 [5] INCS
1A2-12 INCS
11101150 PC 110011101A2-14, 1A2-15, 1A2-16, 1A2-171A2-14
1A2-15
1A2-16 [2+2+2]S
1A2-17 Iterative Suzuki-Miyaura Coupling for Oligo(naphthalene-2,3-diyl)swith a Chiral Terminal Boronyl Group: Synthesis and Control of the Chiral
ConformationGrad. Sch. Eng., Kyoto Univ.ISHIBASHI, Aoi;YAMAMOTO, Takeshi; SUGINOME, Michinori
327 13001400
PC 125013001A2-251A2-25
14101500 PC 140014101A2-32, 1A2-33, 1A2-34, 1A2-351A2-32 Suzuki
1A2-33 Diels-Alder
1A2-34 E
1A2-35* 132
15101600 PC 150015101A2-38, 1A2-40, 1A2-41, 1A2-421A2-38*
1A2-40 C2v
1A2-41
1A2-42 The synthesis of ethynylhelicene oligomers with gunidinium terminusGrad. Sch. Pharm. Sci., Tohoku Univ.SAITO, Nozomi; YAN, Liwei;YAMAGUCHI, Masahiko
16101650 PC 160016101A2-44, 1A2-45, 1A2-46, 1A2-471A2-44 N-(III
1A2-45
1A2-46 4,4--o-
1A2-47 1,2-(5-)
17001750 PC 165017001A2-49, 1A2-50, 1A2-51, 1A2-52,
1A2-531A2-49
1A2-50
1A2-51
1A2-52 p J STCREST
1A2-53
328 900 950
PC 8509002A2-01, 2A2-02, 2A2-03, 2A2-04,2A2-05
2A2-01
2A2-02
2A2-03
2A2-04
2A2-05 Grignard(
10001050 PC 95010002A2-07, 2A2-08, 2A2-09, 2A2-102A2-07
2A2-08
2A2-09 C-Ho-
2A2-10*
-
15
11001150 PC 105011002A2-13, 2A2-15, 2A2-16, 2A2-172A2-13*
2A2-15
2A2-16 3
2A2-17 -Pictet-Spengler
328 13001350
PC 125013002A2-25, 2A2-26, 2A2-27, 2A2-282A2-25 1 Grignard
2A2-26 1
2A2-27 1
2A2-28* Oxidative Dimerization of (Hetero)aromatic Amines Utilizing tert-Butyl Hypoiodite Leading to (Hetero)aromatic Azo CompoundsGrad. Sch.Eng., Osaka Univ.OKUMURA, Sota; LIN, Chun-hsuan; TAKEDA,Youhei; MINAKATA, Satoshi
14001450 PC 135014002A2-31, 2A2-33, 2A2-34, 2A2-352A2-31* Ecient synthesis of multisubstituted benzofurans from phenols byextended Pummerer reactionGrad. Sch. Sci., Kyoto Univ.MURAKAMI,Kei; YORIMITSU, Hideki; OSUKA, Atsuhiro
2A2-33 defucogilvocarcin M
2A2-34
2A2-35 3,3,5,5-
15001550 PC 145015002A2-37, 2A2-38, 2A2-39, 2A2-40,
2A2-412A2-37 N-
2A2-38 BiAr3
2A2-39
2A2-40
2A2-41
16001650 PC 155016002A2-43, 2A2-44, 2A2-45, 2A2-46,
2A2-472A2-43
2A2-44
2A2-45 2
2A2-46
2A2-47 Birch
329 900 950
PC 8509003A2-01, 3A2-02, 3A2-03, 3A2-04,3A2-05
3A2-01 Selective hydrogenation of nitroarenes catalyzed by Pd-based alloy
nanoparticlesWPI-AIMR, Tohoku Univ.; Grad. Sch. Sci., Tohoku Univ.YANG, Lin; ZHAO, Ming; ASAO, Naoki
3A2-02
3A2-03
3A2-04 RC
3A2-05
10001040 PC 95010003A2-07, 3A2-08, 3A2-093A2-07
3A2-08
3A2-09*
10501130 PC 104010503A2-12, 3A2-14, 3A2-153A2-12* RCIS
3A2-14 RCIS
3A2-15 2-
A3 5
C
327
900 1000 PC 8509001A3-01, 1A3-02, 1A3-04, 1A3-05,
1A3-061A3-01
1A3-02*
1A3-04 [4+1]
1A3-05 [3+2]
1A3-06
10101110 PC 100010101A3-08, 1A3-09, 1A3-10, 1A3-12,
1A3-131A3-08 L- Stemaphylline
1A3-09
1A3-10*
1A3-12 1,2,3-
1A3-13 ---
11201220 PC 111011201A3-15, 1A3-16, 1A3-18, 1A3-19,
1A3-201A3-15 1,6-
-
16
1A3-16* Reformatsky
1A3-18 -Michael
1A3-19 C-H
1A3-20
327 13301430
PC 132013301A3-28, 1A3-29, 1A3-30, 1A3-31,1A3-32, 1A3-33
1A3-28 2,3-[3+2]Arteaga Fernando ArteagaNGUYEN Tue Minh-Nhat
1A3-29
1A3-30
1A3-31 2- C2
1A3-32
1A3-33 N-
14401540 PC 143014401A3-35, 1A3-36, 1A3-37, 1A3-38,
1A3-39, 1A3-401A3-35
1A3-36 2-
1A3-37
1A3-38
1A3-39
1A3-40 1,3--5-
15501650 PC 154015501A3-42, 1A3-43, 1A3-44, 1A3-45,
1A3-46, 1A3-471A3-42
1A3-43
1A3-44 PN
1A3-45 E/Z
1A3-46 1,4--1,2,3--5-
1A3-47 2--2- 6
17001740 PC 165017001A3-49, 1A3-50, 1A3-51, 1A3-521A3-49 8, 8-
1A3-50
1A3-51 Mn()
1A3-52 Mn(III)
17501830 PC 174017501A3-54, 1A3-55, 1A3-56, 1A3-57
1A3-54 ,-
1A3-55 1,3--1,3- 1,3-
1A3-56 N-
1A3-57
328 900 1000
PC 8509002A3-01, 2A3-02, 2A3-03, 2A3-04,2A3-06
2A3-01
2A3-02 N- 8 C-H
2A3-03
2A3-04* Asymmetric synthesis and catalytic activities of novel avinium saltsThe University of Toledo Department of ChemistryYAMAMOTO, Kana;ARIMITSU, Kenji; ALMALITI, Jehad
2A3-06
10101110 PC 100010102A3-08, 2A3-10, 2A3-11, 2A3-12,
2A3-132A3-08* SHi
2A3-10 Diels-Alder
2A3-11 8
2A3-12 Furoxan
2A3-13 - 2,3-
11201220 PC 111011202A3-15, 2A3-16, 2A3-17, 2A3-18,
2A3-19, 2A3-202A3-15
2A3-16
2A3-17 Diels-Alder
2A3-18 2--3,1--4- 2--3,1--4-
2A3-19
2A3-20 1,5-
328 13301430
PC 132013302A3-28, 2A3-29, 2A3-30, 2A3-31,2A3-32, 2A3-33
2A3-28 2
2A3-29 2,2--1,1- N-[c]
2A3-30
2A3-31
2A3-32 O- 2,3--[4+2]
-
17
2A3-33 1,3-
329 900 950
PC 8509003A3-01, 3A3-02, 3A3-03, 3A3-053A3-01 3
3A3-02 5-
3A3-03* Synthesis of 2-Aryl-5-nitropyridines by Three Component RingTransformation of 3,5-Dinitro-2-pyridoneKUTLE, Thi song;ASAHARA, Haruyasu; SUGIMOTO, Ryuichi; KOBIRO, Kazuya; SAIGO,
Kazuhiko; NISHIWAKI, Nagatoshi
3A3-05 N-
10001050 PC 95010003A3-07, 3A3-09, 3A3-10, 3A3-113A3-07* Regioselective Rapid Synthesis of Fully Substituted 1,2,3-TriazolesMediated by Propargyl CationsGrad. Sch. Mat. Sci., NAISTZHANG,Huan; TANIMOTO, Hiroki; KAKIUCHI, Kiyomi
3A3-09 N-
3A3-10 1,3,5-[1,5-a]
3A3-11 [1,5-a]
11001150 PC 105011003A3-13, 3A3-15, 3A3-16, 3A3-173A3-13* tert- C4h
3A3-15 1,3,4-
3A3-16
3A3-17
A
329
13101410 PC 130013103A3-26, 3A3-28, 3A3-30, 3A3-313A3-26* Synthesis and Characterization of Rotaxanes Possessing ThermallyDegradable CounteranionsGrad. Sch. Sci., Eng., Tokyo TechZHU, Nan;ABE, Yoko; NAKAZONO, Kazuko; TAKATA, Toshikazu
3A3-28*
3A3-30 NMRPhan Son Thanh
3A3-31
14201510 PC 141014203A3-33, 3A3-35, 3A3-36, 3A3-373A3-33* Novel cyclic amide oligomer containing pi-conjugated unit: Designand chiral characterizationNagoya Inst. of Tech. Grad. School of Eng.YAMAKADO, Ryohei; MATSUOKA, Sin-ichi; SUZUKI, Masato;
TAKAGI, Koji; MASU, Hyuma; TAKEUCHI, Daisuke; AZUMAYA, Isao
3A3-35 2-
3A3-36 9,10-
3A3-37
15201620 PC 151015203A3-39, 3A3-41, 3A3-42, 3A3-43,
3A3-443A3-39*
3A3-41 S X
3A3-42
3A3-43
3A3-44 JST CREST
330 900 1000
PC 8509004A3-01, 4A3-02, 4A3-03, 4A3-04,4A3-05, 4A3-06
4A3-01
4A3-02 MAURIZOTVictor HUC Ivan
4A3-03 4,8-
4A3-04
4A3-05
4A3-06 [6]Cycloparaphenylene
10101110 PC 100010104A3-08, 4A3-10, 4A3-11, 4A3-12,
4A3-134A3-08* Conformational Analysis of Single Peruoroalkyl Chains by Single-Molecule Real-Time Transmission Electron Microscopic ImagingGrad. Sch.Sci., The Univ. of Tokyo; NTRC, AISTHARANO, Koji; TAKENAGA,Shinya; OKADA, Satoshi; NIIMI, Yoshiko; YOSHIKAI, Naohiko; ISOBE,
Hiroyuki; SUENAGA, Kazu; KATAURA, Hiromichi; KOSHINO, Masanori;
NAKAMURA, Eiichi
4A3-10 CH/
4A3-11 X
4A3-12 JST CREST
4A3-13 XJST
11201200 PC 111011204A3-15, 4A3-16, 4A3-17, 4A3-184A3-15 MiranMohammed
4A3-16 UV-vis
4A3-17 DPPH Cl
4A3-18
A4 1
A
327
10101110 PC 100010101A4-08, 1A4-09, 1A4-10, 1A4-11,
1A4-121A4-08
1A4-09 25
-
18
1A4-10
1A4-11 ()
1A4-12* (AIE) (PeT)
11201220 PC 111011201A4-15, 1A4-17, 1A4-18, 1A4-19,
1A4-201A4-15* Environment-Responsive Fluorescent Probe Containing a PhospholeOxideGrad. Sch. Sci., Nagoya Univ.YAMAGUCHI, Eriko;FUKAZAWA, Aiko; KOSAKA, Youhei; SATO, Yoshikatsu; SASAKI,
Taeko; UEDA, Minako; SASAKI, Narie; HIGASHIYAMA, Tetsuya;
YAMAGUCHI, Shigehiro
1A4-17 2,5- ESIPTWPI-ITbM
1A4-18
1A4-19 1,8-(-1-)
1A4-20 1-Acetylaminopyrene
327 13301430
PC 132013301A4-28, 1A4-29, 1A4-30, 1A4-31,1A4-32, 1A4-33, 2A4-28, 2A4-29, 2A4-30, 2A4-31, 2A4-32
1A4-28
1A4-29 (CPL)
1A4-30 (CPL)
1A4-31 (CPL)
1A4-32
1A4-33
B
328
133014202A4-28 -1,3-
2A4-29
2A4-30 ALCA,JST
2A4-31 2--3--(E)--1-
2A4-32 5-exo6-endo
14301530 PC 142014302A4-34, 2A4-36, 2A4-37, 2A4-382A4-34* Si-Si[2 + 1]
2A4-36 [2+2]
2A4-37 4,4-1,2--3,5-
2A4-38*
15401630 PC 153015402A4-41, 2A4-42, 2A4-43, 2A4-44,
2A4-452A4-41 -
2A4-42 : 31P NMR
2A4-43
2A4-44 C-C-
2A4-45
16401730 PC 163016402A4-47, 2A4-49, 2A4-502A4-47* Decoration of Porous Coordination Polymers with Nitroxyl Radicalsfor Selectively Catalytic Oxidation of AlcoholsiCeMS, Kyoto Univ.LI,Liangchun; MATSUDA, Ryotaro; KITAGAWA, Susumu
2A4-49
2A4-50*
Asian International Symposium-Photochemistry-
329
100010103A4-07 Opening addressOsaka UniversityMajima, Tetsuro10:0010:10
Chair: Ohta, Nobuhiro101010503A4-08 Keynote Lecture Studies of unimolecular photodissociationdynamics using synchrotron VUV ionizationNSRRCLee, Shih-Huang10:1010:50
Chair: Tamai, Naoto111011503A4-14 Invited Lecture Functionalization of titanium oxide by metalcomplex modication and its application to energy and molecular transforma-
tionsKyushu UniversityShimakoshi, Hisashi11:1011:303A4-16 Invited Lecture Photoswitching of biological functions based onthe photoisomerization of azobenzenesHokkaido UniversityFukaminato,Tsuyoshi11:3011:50
329Chair: Karatsu, Takashi13001340
3A4-25 Keynote Lecture Optical gain in strongly quantum connedcolloidal semiconductor nanostructuresNational University of SingaporeChan, Yin Thai13:0013:40
Chair: Arai, Tatsuo140014403A4-31 Invited Lecture Developing Metal-Polycyclic-Aromatic-Hydro-carbons Into a New Class of Organometallic Emitters and Photosensitizers
National University of SingaporeYip, John H. K.14:0014:40
Chair: Majima, Tetsuro150016003A4-37 Keynote Lecture Eco-driven environmetal remediation and H2generation based on photocatalytic and photoelectrocatalytic techniques
Shanghai Normal UniversityLi, Guisheng15:0015:403A4-41 Invited Lecture Design and application of TiO2-based photo-functional materialsOsaka UniversityKamegawa, Takashi15:4016:00
Chair: Yasuda, Masahide162017303A4-45 Invited Lecture DNA scaolded chromophore aggregates andtheir photochemical behaviorUniversity of HyogoNakamura, Mitsunobu16:2016:40
3A4-47 Invited Lecture Photosensitized damage of DNA and proteinShizuoka UniversityHirakawa, Kazutaka16:4017:00
3A4-49 Invited Lecture Thermoswitchable Emission and Colora-tion of a Composite Material Containing a Luminescent Lantha-
nide(III) Complex and Fluoran DyeChiba UniversityNakamura, Kazuki17:0017:20
3A4-51 Closing addressNational University of SingaporeYip, John H. K.17:2017:30
-
19
A
330
900 1000 PC 8509004A4-01, 4A4-02, 4A4-03, 4A4-04,
4A4-05, 4A4-064A4-01
4A4-02
4A4-03 Push-pull 1,5-
4A4-04 1,8-
4A4-05 / OPERA
4A4-06
10101110 PC 100010104A4-08, 4A4-10, 4A4-11, 4A4-12,
4A4-134A4-08* Didier PascalMely YvesKlymchenko Andrey
4A4-10
4A4-11
4A4-12 2-()
4A4-13 [2.2]
11201220 PC 111011204A4-15, 4A4-17, 4A4-18, 4A4-19,
4A4-204A4-15* Nonlinear Optical Eects related to Aromatic Polyimide Conforma-tionGrad. Sch. Sci., Eng., Tokyo TechSHIRATA, Kei; HATTORI,Masaya; MIYAWAKI, Ryousuke; KAWAUCHI, Susumu
4A4-17 (4) CMSJST-CREST
4A4-18 (5) CMSJST-CREST
4A4-19 N,N-/OPERA
4A4-20 EL
330
13301410 PC 132013304A4-28, 4A4-29, 4A4-304A4-28
4A4-29 J
4A4-30* Synthesis of diyne-labeled sphingomyelin and evaluation of its raft-likedomain formationSch. Sci., Osaka Univ.CUI, Jin; KINOSHITA,Masanao; MATSUOKA, Shigeru; SATO, Fuminori; ANDO, Jun;
YAMAGOSHI, Hiroyuki; DODO, Koyuke; FUJITA, Katsumasa;
SODEOKA, Mikio; MURATA, Michio
14201450 PC 141014204A4-33, 4A4-34, 4A4-354A4-33 -
4A4-34
4A4-35
15001520 PC 145015004A4-37, 4A4-384A4-37
4A4-38
15301550 PC 152015304A4-40, 4A4-414A4-40
4A4-41
A5 2
A
327
900 940 PC 8509001A5-01, 1A5-02, 1A5-031A5-01
1A5-02
1A5-03* Porous Molecular Networks on Graphene Formed by Self-Assemblyof Dehydrobenzo[12]annulene DerivativesGrad. Sch. Eng. Sci., Osaka Univ.;JST-PRESTO; KU Leuven-University of Leuven Department of Chemistry,TAHARA, Kazukuni; LI, Bing; ADISOEJOSO, Jinne; VANDERLINDEN,
Willem; DE GENDT, Stefan; DE FEYTER, Steven; TOBE, Yoshito
950 1030 PC 9409501A5-06, 1A5-081A5-06*
1A5-08* /MANA/WPI-MANA
10401120 PC 103010401A5-11, 1A5-13, 1A5-141A5-11* WPI-TIbMJST-JST-CREST
1A5-13
1A5-14
11301200 PC 112011301A5-16, 1A5-17, 1A5-181A5-16 MOF
1A5-17
1A5-18 -
12101230 PC 120012101A5-20, 1A5-211A5-20 8 -
-
20
1A5-21
327 13401410
PC 133013401A5-29, 1A5-30, 1A5-311A5-29
1A5-30
1A5-31
14201440 PC 141014201A5-33, 1A5-341A5-33
1A5-34
17001740 PC 165017001A5-49, 1A5-51, 1A5-521A5-49* (1) CMSJST CRESTMahato Prasenjit
1A5-51 (2)
1A5-52 (3) CMSJST CREST
17501830 PC 174017501A5-54, 1A5-55, 1A5-561A5-54 //SiO2-TiO2
1A5-55
1A5-56*
328
900 940 PC 8509002A5-01, 2A5-02, 2A5-032A5-01
2A5-02
2A5-03* Molecular recognition controlled by remote substituents on self-assembled hollow cagesGrad. Sch. Eng., The Univ. of TokyoFANG, Yu;MURASE, Takashi; FUJITA, Makoto
950 1030 PC 9409502A5-06, 2A5-082A5-06*
2A5-08*
10401110 PC 103010402A5-112A5-11 X
11201150 PC 111011202A5-15, 2A5-16, 2A5-172A5-15 XJST CREST
2A5-16 Stable encapsulation of acrylate esters within networked capsulesGrad. Sch. Eng., The Univ. of TokyoNING, Guo-hong; INOKUMA,Yasuhide; FUJITA, Makoto
2A5-17
12001230 PC 115012002A5-19, 2A5-20, 2A5-212A5-19
2A5-20
2A5-21 Pd(II)
328 13401420
PC 133013402A5-29, 2A5-30, 2A5-322A5-29
2A5-30*
2A5-32
14301510 PC 142014302A5-34, 2A5-35, 2A5-362A5-34 4-
2A5-35
2A5-36*
15201550 PC 151015202A5-39, 2A5-40, 2A5-412A5-39 TPEN-Nd(III)
2A5-40
2A5-41
16001640 PC 155016002A5-43, 2A5-45, 2A5-462A5-43* PEG
2A5-45
2A5-46 Au8
16501730 PC 164016502A5-48, 2A5-50, 2A5-512A5-48* Development of macrocyclic host molecules based on dynamicoctadentate cyclen-metal complexesGrad. Sch. Sci., Osaka City Univ.ITO, Hiroshi; SHINODA, Satoshi
2A5-50 3,7-
2A5-51
329
900 930 PC 8509003A5-01, 3A5-02, 3A5-033A5-01
3A5-02
3A5-03
940 1020 PC 9309403A5-05, 3A5-07, 3A5-083A5-05*
3A5-07 :
3A5-08 :
-
21
10301100 PC 102010303A5-10, 3A5-11, 3A5-123A5-10 6
3A5-11 2,2,3,3--1,1-
3A5-12
11101140 PC 110011103A5-14, 3A5-15, 3A5-163A5-14 (II)
3A5-15
3A5-16
11501230 PC 114011503A5-18, 3A5-20, 3A5-213A5-18* Carbon nanorings as porous materialsENCs, Shinshu Univ.SAKAMOTO, Hirotoshi; FUJIMORI, Toshihiko; LI, Xiaolin; KANEKO,
Katsumi
3A5-20
3A5-21
329 13401410
PC 133013403A5-29, 3A5-30, 3A5-313A5-29 anti-O,O--p-H-[4]
3A5-30 m-
3A5-31
14201450 PC 141014203A5-33, 3A5-34, 3A5-353A5-33
3A5-34
3A5-35
15001610 PC 145015003A5-37, 3A5-38, 3A5-39, 3A5-40,
3A5-42, 3A5-433A5-37 2,5-(1,3--2-)-1,3--4-
3A5-38 EL
3A5-39 OLED/OPERA I2CNERPotscavage William
3A5-40* V
3A5-42 W
3A5-43 / OPERAYang Yu Seok
16201720 PC 161016203A5-45, 3A5-46, 3A5-47, 3A5-48,
3A5-49, 3A5-503A5-45 WPI-AIMR
3A5-46 n-WPI-AIMR
3A5-47 WPI-AIMR
3A5-48 :
3A5-49 D--AJST
3A5-50 JST
17301830 PC 172017303A5-52, 3A5-53, 3A5-54, 3A5-55,
3A5-56, 3A5-573A5-52
3A5-53
3A5-54
3A5-55 n
3A5-56
3A5-57 s-
330 900 950
PC 8509004A5-01, 4A5-02, 4A5-03, 4A5-054A5-01
4A5-02
4A5-03* Synthesis and properties of - extended derivatives of sumanene IMSSHRESTHA, B i nod babu ; KARANJ IT , S an g i t a ;HIGASHIBAYASHI, Shuhei; SAKURAI, Hidehiro
4A5-05 Shrestha Binod Babu
10001050 PC 95010004A5-07, 4A5-08, 4A5-09, 4A5-10,
4A5-114A5-07 [9]
4A5-08
4A5-09 JST
4A5-10 C70
4A5-11 Synthesis and Properties of HydroxysumaneneIMSNGAMSOMPRASERT, Niti; HIGASHIBAYASHI, Shuhei; SAKURAI,
Hidehiro; SHRESTHA, Binod babu
11001150 PC 105011004A5-13, 4A5-14, 4A5-15, 4A5-164A5-13 (I)
4A5-14
4A5-15
4A5-16*
-
22
12001250 PC 115012004A5-19, 4A5-20, 4A5-21, 4A5-224A5-19
4A5-20
4A5-21
4A5-22* N-H[5]
330
14101500 PC 140014104A5-32, 4A5-34, 4A5-35, 4A5-364A5-32* WPI-ITbMJST CRESTJST
4A5-34 9--10-
4A5-35 4, 7 2-
4A5-36
15101600 PC 150015104A5-38, 4A5-39, 4A5-40, 4A5-41,
4A5-424A5-38 JST-PRESTO
4A5-39 JST-PRESTO
4A5-40 JST-PRESTO
4A5-41
4A5-42 DSSC
16101700 PC 160016104A5-44, 4A5-45, 4A5-46, 4A5-47,
4A5-484A5-44 JST-PRESTO
4A5-45 2WPI-ITbMJST CRESTJSTDOU Chouandong
4A5-46 2
4A5-47
4A5-48
A6 3
A
327
900 1000 PC 8509001A6-01, 1A6-02, 1A6-03, 1A6-04,
1A6-05, 1A6-061A6-01
1A6-02
1A6-03 ESR
1A6-04 Cr()N
1A6-05
1A6-06
10101110 PC 100010101A6-08, 1A6-09, 1A6-10, 1A6-11,
1A6-12, 1A6-131A6-08
1A6-09 WPI-ITbM
1A6-10
1A6-11 Syntheses and properties of uorenyl-based hydrocarbon radicalsGrad. Sch. Sci., Osaka Univ.TIAN, Ti; KURATA, Hiroyuki;NISHIUCHI, Tomohiko; HIRAO, Yasukazu; KUBO, Takashi
1A6-12 2
1A6-13
11201220 PC 111011201A6-15, 1A6-16, 1A6-17, 1A6-18,
1A6-19, 1A6-201A6-15
1A6-16
1A6-17 FET
1A6-18
1A6-19 JST CREST
1A6-20 JST CREST
327 13301430
PC 132013301A6-28, 1A6-30, 1A6-321A6-28* Ln(III)
1A6-30* /
1A6-32* HOFFMANN ROALD
17001730 PC 165017001A6-491A6-49 OPERA I2CNERJST
17401850 PC 173017401A6-53, 1A6-55, 1A6-56, 1A6-57,
1A6-591A6-53* - BTBT-
1A6-55 JST
1A6-56 N-Boc
1A6-57* (1):
1A6-59 (2):
-
23
328
900 1000 PC 8509002A6-01, 2A6-02, 2A6-03, 2A6-04,
2A6-05, 2A6-062A6-01 CPP
2A6-02
2A6-03 Pillar[5]arene
2A6-04
2A6-05 SPM-
2A6-06
10101110 PC 100010102A6-08, 2A6-09, 2A6-11, 2A6-12,
2A6-132A6-08 31N-
2A6-09* A Bis(2-hydroxyphenyl)pyrimidine-bridged Multiple Molecular SpurGears: Synthesis and Dynamic Motions.Chem. Res. Lab., Tokyo TechTSUCHIDO, Yoshitaka; SUZAKI, Yuji; OSAKADA, Kohtaro
2A6-11
2A6-12
2A6-13
11201220 PC 111011202A6-15, 2A6-16, 2A6-17, 2A6-18,
2A6-19, 2A6-202A6-15 4
2A6-16 3 3
2A6-17
2A6-18
2A6-19
2A6-20
328 13301430
PC 132013302A6-28, 2A6-29, 2A6-30, 2A6-31,2A6-32, 2A6-33
2A6-28
2A6-29
2A6-30
2A6-31
2A6-32
2A6-33 [3+2]
14401540 PC 143014402A6-35, 2A6-36, 2A6-37, 2A6-39,
2A6-402A6-35 JST CREST
2A6-36 (1)
2A6-37* (2)
2A6-39
2A6-40
15501650 PC 154015502A6-42, 2A6-43, 2A6-44, 2A6-45,
2A6-472A6-42
2A6-43 M12L24
2A6-44 MnL2n
2A6-45* Supramolecular Corannulene FiberRIKEN CEMSMIYAJIMA,Daigo; KANG, Jiheong; AIDA, Takuzo
2A6-47
17001730 PC 165017002A6-49, 2A6-50, 2A6-512A6-49
2A6-50
2A6-51
329 900 1000
PC 8509003A6-01, 3A6-02, 3A6-04, 3A6-063A6-01 Pillar[5]arene
3A6-02* Synthesis of the [3]Rotaxanes Utilizing the Catalytic Activity of theMacrocyclic Phenanthroline-Cu ComplexGrad. Sch. Chem. Sci. Technol.,Tokyo Univ. of Sci.YAMASHITA, Yoshiaki; MUTOH, Yuichiro;YAMASAKI, Ryu; KASAMA, Takeshi; SAITO, Shinichi
3A6-04* [3]
3A6-06
10101110 PC 100010103A6-08, 3A6-09, 3A6-10, 3A6-123A6-08
3A6-09
3A6-10*
3A6-12*
11201220 PC 111011203A6-15, 3A6-16, 3A6-17, 3A6-18,
3A6-203A6-15 [2]YOUNG Philip G.
3A6-16
3A6-17 C2
3A6-18*
-
24
3A6-20
329 13301430
PC 132013303A6-28, 3A6-29, 3A6-30, 3A6-32,3A6-33
3A6-28 (1)()
3A6-29 (2)()
3A6-30*
3A6-32 1 Pillar[5]arene
3A6-33
14401540 PC 143014403A6-35, 3A6-37, 3A6-38, 3A6-393A6-35* La@C82SLANINA ZdenekGuoJingdong
3A6-37 Halim Md. Ershad
3A6-38
3A6-39* -[4+4]//JST CREST
15501650 PC 154015503A6-42, 3A6-44, 3A6-46, 3A6-473A6-42* VBL
3A6-44*
3A6-46
3A6-47
17001800 PC 165017003A6-49, 3A6-51, 3A6-52, 3A6-53,
3A6-543A6-49* Extraction of Pd(II) ions with dimethyl(thiocarbamoyl) modifiedthiacalix[n]arenesFac. Eng. Resource Sci., Akita Univ.MUNIYAPPAN,Rajiv gandhi; YAMADA, Manabu; KONDO, Yoshihiko; HAMADA, Fumio
3A6-51
3A6-52 ---[24]-8-
3A6-53
3A6-54
18101830 PC 180018103A6-56, 3A6-573A6-56 Esipenko NinaAnzenbacher Jr Pavel
3A6-57
330 900 1000
PC 8509004A6-01, 4A6-02, 4A6-03, 4A6-05,4A6-06
4A6-01
4A6-02
4A6-03* -
4A6-05 MRI TEMPO
4A6-06
10101110 PC 100010104A6-08, 4A6-09, 4A6-10, 4A6-11,
4A6-12, 4A6-134A6-08
4A6-09
4A6-10
4A6-11
4A6-12
4A6-13
11201220 PC 111011204A6-15, 4A6-16, 4A6-18, 4A6-19,
4A6-204A6-15
4A6-16*
4A6-18
4A6-19 1,9,10- Tweezers
4A6-20 Pillar[5]arene
330 13301430
PC 132013304A6-28, 4A6-30, 4A6-31, 4A6-32,4A6-33
4A6-28*
4A6-30
4A6-31
4A6-32 /
4A6-33
14401540 PC 143014404A6-35, 4A6-36, 4A6-38, 4A6-39,
4A6-404A6-35 Au(I)
4A6-36* Self-Assembly of Boroxine CagesGrad. Sch. Sci., Eng., Tokyo Tech;JST CRESTONO, Kosuke; IWASAWA, Nobuharu
4A6-38
4A6-39
4A6-40
15501640 PC 154015504A6-42, 4A6-43, 4A6-44, 4A6-45,
4A6-46
-
25
4A6-42 m-
4A6-43
4A6-44
4A6-45 1
4A6-46 2
A7 5 12
A
327
900 1000 PC 8509001A7-01, 1A7-02, 1A7-03, 1A7-04,
1A7-05, 1A7-061A7-01 -
1A7-02
1A7-03
1A7-04
1A7-05 2,8- 2,9-
1A7-06
10101100 PC 100010101A7-08, 1A7-09, 1A7-10, 1A7-121A7-08 JST
1A7-09 JST
1A7-10* [2.2]
1A7-12
11101210 PC 110011101A7-14, 1A7-15, 1A7-16, 1A7-17,
1A7-181A7-14 S-
1A7-15 [5,3][3,3]
1A7-16
1A7-17
1A7-18* [20][30]
327 13201400
PC 131013201A7-27, 1A7-29, 1A7-301A7-27* Five-Fold Symmetric Penta-Bioconjugated Corannulenes: Synthesis,Properties and ApplicationsTohoku Univ. Department of Chemistry andWPI-AIMRMATTARELLA, Martin; SIEGEL, Jay
1A7-29 9,10-()
1A7-30 Syntheses and Structual Characterization of Pyrene-Based MetalComplexesGrad. Sch. Sci. Eng., Tokyo Metropolitan Univ.LUONG,Xuan-dien; YAMASHITA, Ken-ichi; ASANO, Motoko; SUGIURA, Ken-ichi
14101450 PC 140014101A7-32, 1A7-33, 1A7-34, 1A7-351A7-32
1A7-33
1A7-34
1A7-35 [3.3.3]
17101800 PC 170017101A7-50, 1A7-52, 1A7-53, 1A7-541A7-50*
1A7-52 WPI-ITbMJST ERATOSibbel FriederikeStuder Armido
1A7-53 [N]
1A7-54 [N]
18101900 PC 180018101A7-56, 1A7-57, 1A7-58, 1A7-591A7-56 ZHAIXue
1A7-57 3,14-
1A7-58 5,12-
1A7-59*
328
900 1000 PC 8509002A7-01, 2A7-02, 2A7-03, 2A7-05,
2A7-062A7-01
2A7-02 DA
2A7-03*
2A7-05 9,10-
2A7-06
10101110 PC 100010102A7-08, 2A7-09, 2A7-10, 2A7-112A7-08
2A7-09
2A7-10
2A7-11
11201220 PC 111011202A7-15, 2A7-16, 2A7-17, 2A7-19,
2A7-202A7-15
2A7-16 1,3-[5]
2A7-17* 1,3-[5]
2A7-19 3,7-
2A7-20 [4n]
-
26
328 13301420
PC 132013302A7-28, 2A7-29, 2A7-30, 2A7-31,2A7-32
2A7-28 D-A
2A7-29 -
2A7-30
2A7-31
2A7-32
14301520 PC 142014302A7-34, 2A7-37, 2A7-382A7-34 //
2A7-37 [2.2] TTF
2A7-38 [2.2]
15301620 PC 152015302A7-40, 2A7-41, 2A7-42, 2A7-43,
2A7-442A7-40
2A7-41 [16]
2A7-42 2,5-2-
2A7-43 1
2A7-44 2
16301720 PC 162016302A7-46, 2A7-47, 2A7-48, 2A7-49,
2A7-502A7-46 C-H-
2A7-47
2A7-48
2A7-49 D--A
2A7-50
329
900 1000 PC 8509003A7-01, 3A7-03, 3A7-05, 3A7-063A7-01* Scott Lawrence
3A7-03* [3+2]
3A7-05 -
3A7-06 2 1,3-
10101100 PC 100010103A7-08, 3A7-10, 3A7-11, 3A7-123A7-08*
3A7-10 C60 XJST
3A7-11 13 C70JST
3A7-12 C60JST
11101210 PC 110011103A7-14, 3A7-15, 3A7-16, 3A7-17,
3A7-183A7-14 3
3A7-15 3()/
3A7-16
3A7-17
3A7-18*
329 13201420
PC 131013203A7-27, 3A7-28, 3A7-29, 3A7-30,3A7-31, 3A7-32
3A7-27
3A7-28
3A7-29
3A7-30 opp-
3A7-31
3A7-32
14301530 PC 142014303A7-34, 3A7-35, 3A7-37, 3A7-38,
3A7-393A7-34
3A7-35* -
3A7-37
3A7-38 JST CREST
3A7-39
15401640 PC 153015403A7-41, 3A7-43, 3A7-44, 3A7-45,
3A7-463A7-41*
3A7-43 44
3A7-44 5,10-()
3A7-45
3A7-46 ABC
16501750 PC 164016503A7-48, 3A7-49, 3A7-50, 3A7-51,
3A7-52, 3A7-533A7-48
3A7-49 -
-
27
3A7-50
3A7-51
3A7-52
3A7-53
18001850 PC 175018003A7-55, 3A7-57, 3A7-58, 3A7-593A7-55* Two Terminal Wired Single Molecular Diodes of Porphyrin-ImideConnected to Single-Walled Carbon NanotubesOsaka Univ.MURNI,Handayani; GODA, Shun; TANAKA, Hirofumi; TANAKA, Daisuke;
KATAYOSE, Shinichi; OGAWA, Takuji
3A7-57 meso-
3A7-58
3A7-59 -
330
900 950 PC 8509004A7-01, 4A7-02, 4A7-034A7-01
4A7-02
4A7-03
10001050 PC 95010004A7-07, 4A7-08, 4A7-09, 4A7-10,
4A7-114A7-07 8 3WPI-ITbM JST- JST-CREST YUAN ChunxueCAMACHO CristopherIRLE Stephane
4A7-08 PCET
4A7-09
4A7-10 1H-[de]-4,5-()
4A7-11
11001150 PC 105011004A7-13, 4A7-14, 4A7-15, 4A7-164A7-13
4A7-14
4A7-15
4A7-16* [n]
330 13001350
PC 125013004A7-25, 4A7-26, 4A7-27, 4A7-284A7-25
4A7-26 5,11-[3,2-b]
4A7-27 [a,j]
4A7-28* 2,5-[()]-1,4-
14001450 PC 135014004A7-31, 4A7-32, 4A7-33, 4A7-34,
4A7-354A7-31 2,3-(1-)-1,3- Diels-Alder
4A7-32
4A7-33 BODIPY
4A7-34 [3,2-b]Truong Minh Anh
4A7-35 [1,2-b:4,5-b]
15001600 PC 145015004A7-37, 4A7-38, 4A7-39, 4A7-40,
4A7-41, 4A7-424A7-37
4A7-38
4A7-39
4A7-40
4A7-41
4A7-42
16101650 PC 160016104A7-44, 4A7-45, 4A7-464A7-44 1
4A7-45 2
4A7-46* Ion Conductivity of Multi-interactive TPHAP Derivatives Based onTheir Assembled StructuresPOSTECHYAKIYAMA, Yumi; LEE, Gil-ryeong; MORITA, Yasushi; KAWANO, Masaki
B1 ES101(ES)
E
327
B
900 1000 PC 8509001B1-01, 1B1-02, 1B1-03, 1B1-04,
1B1-05, 1B1-061B1-01 Enantioselective Synthesis of -Chiral (E)--Alkoxyallylboronatesvia Copper(I)-Catalyzed Nucleophilic -Boryl-Substitution of Allyl AcetalsGrad. Sch. Chi Sci. and Eng., Hokkaido Univ.TAKENOUCHI, Yuta;YAMAMOTO, Eiji; OZAKI, Taichi; ITO, Hajime
1B1-02 Enantioselective Monoborylation of Alkenylsilanes Catalyzed by aChiral Phosphine-Copper(I) ComplexGrad. Sch. Chi Sci. and Eng.,Hokkaido Univ.KUBOTA, Koji; YAMAMOTO, Eiji; ITO, Hajime
1B1-03
1B1-04 (I)
1B1-05 (I)
1B1-06
-
28
10101110 PC 100010101B1-08, 1B1-09, 1B1-11, 1B1-12,
1B1-131B1-08
Si
1B1-09* GRRM/AFIR:
B
1B1-11
Al
1B1-12 Splitting water with aluminum porphyrinsUrban EnvironmentalSci., Tokyo Metropolitan Univ.KUTTASSERY, Fazalurahman;SAGAWA, Shogo; MATHEW, Siby; YAMAMOTO, Daisuke; ONUKI,
Satomi; NABETANI, Yu; TACHIBANA, Hiroshi; INOUE, Haruo
1B1-13 Synthesis and spectroscopic studies of Aluminum porphyrinsUrbanEnvironmental Sci., Tokyo Metropolitan Univ.MATHEW, Siby;KUTTASSERY, Fazalurahman; ONUKI, Satomi; YAMAMOTO, Daisuke;
NABETANI, Yu; TACHIBANA, Hiroshi; INOUE, Haruo
Cu
11201220 PC 111011201B1-15, 1B1-16, 1B1-17, 1B1-18,
1B1-19, 1B1-201B1-15 2,3-
1B1-16 O, N
1B1-17 O-
1B1-18 1,4-
1B1-19
1B1-20
327 13401440
PC 133013401B1-291B1-29
17001800 PC 165017001B1-49, 1B1-50, 1B1-51, 1B1-52,
1B1-53, 1B1-541B1-49 ,- Karan Bobuatong
1B1-50 N-
1B1-51
1B1-52 Cu
1B1-53
1B1-54
328 900 1000
PC 8509002B1-01, 2B1-02, 2B1-03, 2B1-04,2B1-05, 2B1-06
2B1-01 //
2B1-02 - -
2B1-03 1
2B1-04
2B1-05
2B1-06 Cu(I) 1,2-
10101110 PC 100010102B1-08, 2B1-10, 2B1-11, 2B1-122B1-08* Copper-Catalyzed Intramolecular Oxidative C(sp3)-H and C(sp2)-HAmidationGrad. Sch. Pharm., The Univ. of Tokyo; The Univ. of TokyoERATO-JSTWANG, Zhen; KUNINOBU, Yoichiro; KANAI, Motomu
2B1-10 Mizoroki-Heck
2B1-11 -
2B1-12*
11201220 PC 111011202B1-15, 2B1-16, 2B1-17, 2B1-18,
2B1-19, 2B1-202B1-15
2B1-16
-
29
2B1-17
2B1-18 C(sp3)-HERATO-JST
2B1-19
2B1-20 O-
328
Fe
13301430 PC 132013302B1-28, 2B1-29, 2B1-30, 2B1-322B1-28 CAZBOX
2B1-29
2B1-30* Aryl C-Glycoside Synthesis Based on Iron-Catalyzed Cross-CouplingReaction of Arylzinc ReagentsGrad. Sch. Eng., Kyoto Univ.; ICR, KyotoUniv.ADAK, Laksmikanta; KAWAMURA, Shintaro; TOMA, Gabriel; LI,Ho Chuen; TAKENAKA, Toshio; ISOZAKI, Katsuhiro; TAKAYA, Hikaru;
SHING, Tony K. M.; NAKAMURA, Masaharu
2B1-32* Iron-Catalyzed Directed Coupling of C(sp2)-H Bond with Organo-boron CompoundsGrad. Sch. Sci., The Univ. of TokyoSHANG, Rui;ILIES, Laurean; NAKAMURA, Eiichi
14401540 PC 143014402B1-35, 2B1-36, 2B1-37, 2B1-38,
2B1-39, 2B1-402B1-35 CH
2B1-36 C-HGHORAI Sujit. K
2B1-37 GOWER N. J.ADAK Laksmikanta
2B1-38 /
2B1-39 Iron-Catalyzed Suzuki-Miyaura Cross-Coupling between Alkyl Ha-lides and Alkynylborate ReagentsICR, Kyoto Univ.; Grad. Sch. Eng.,Kyoto Univ.NAKAGAWA, Naohisa; HATAKEYAMA, Takuji;NAKAMURA, Masaharu
2B1-40 -NHC
15501630 PC 154015502B1-42, 2B1-43, 2B1-44, 2B1-452B1-42
2B1-43
2B1-44 Grignard
2B1-45 Grignard
16401720 PC 163016402B1-47, 2B1-48, 2B1-49, 2B1-502B1-47
2B1-48
2B1-49 DMF
2B1-50 1,6-[2+2+2]
329
Zn
910 1000 PC 9009103B1-02, 3B1-04, 3B1-05, 3B1-063B1-02* Development of Catalytic Allylation Reactions Using Zinc AmidesGrad. Sch. Sci., The Univ. of TokyoYAMASHITA, Yasuhiro; CUI, Yi;KOBAYASHI, Shu
3B1-04 CUI Yi
3B1-05 Tunable Zinc Amide-catalyzed Reactions: Selective Synthesis ofAllenylic and Propargylic AlcoholsGrad. Sch. Sci., The Univ. of TokyoXIE, Peizhong; CUI, Yi; YAMASHITA, Yasuhiro; KOBAYASHI, Shu
3B1-06
10101110 PC 100010103B1-08, 3B1-09, 3B1-10, 3B1-11,
3B1-133B1-08
3B1-09
Ni
3B1-10
3B1-11*
3B1-13
11201220 PC 111011203B1-153B1-15
329
Cu
13301430 PC 132013303B1-28, 3B1-31, 3B1-32, 3B1-333B1-28
Ni
3B1-31
3B1-32
3B1-33
Cu
14401540 PC 143014403B1-35, 3B1-36, 3B1-38, 3B1-39,
3B1-403B1-35 4
3B1-36* IMRENUS
3B1-38 1
3B1-39 2
3B1-40 (3):
-
30
15501650 PC 154015503B1-42, 3B1-43, 3B1-44, 3B1-45,
3B1-46, 3B1-473B1-42 2
3B1-43
3B1-44 (I)
3B1-45 DMF
3B1-46
3B1-47
17001800 PC 165017003B1-49, 3B1-50, 3B1-51, 3B1-52,
3B1-53, 3B1-543B1-49
3B1-50
3B1-51
3B1-52 Bis(NHC)-Cu
3B1-53 1,3-
3B1-54 ()
330
Co
910 1000 PC 9009104B1-02, 4B1-03, 4B1-054B1-02 N-()
4B1-03* Co-Catalyzed Cross-Coupling of Alkyl Halides with Tertiary AlkylGrignard Reagents Using a 1,3-Butadiene AdditiveGrad. Sch. Eng., OsakaUniv.; CSIR Indian Institute of Chemical Technology Inorganic andPhysical Chemistry DivisionIWASAKI, Takanori; TAKAGAWA, Hiroaki;SINGH, Surya p.; KUNIYASU, Hitoshi; KAMBE, Nobuaki
4B1-05* Cobalt-Catalyzed C4-Selective Alkylation of Pyridines and QuinolinesGrad. Sch. Pharm., The Univ. of TokyoYAMAMOTO, Shohei; SAGA,Yutaka; ANDOU, Takashi; MATSUNAGA, Shigeki; KANAI, Motomu
Ni
10101110 PC 100010104B1-08, 4B1-09, 4B1-11, 4B1-134B1-08 Ni(0)
4B1-09*
4B1-11* Nickel-Catalyzed C-H/C-O Biaryl Coupling: Catalyst Developmentand Mechanistic StudyGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTMUTO, Kei; YAMAGUCHI, Junichiro; ITAMI,Kenichiro
4B1-13 Ni-Catalyzed Direct Coupling of Carbonyls and Phenol DerivativesGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTTAKISE, Ryosuke; MUTO, Kei; YAMAGUCHI, Junichiro; ITAMI,
Kenichiro
11201220 PC 111011204B1-15, 4B1-16, 4B1-17, 4B1-18,
4B1-19, 4B1-204B1-15 --
4B1-16 -
4B1-17 Ni(0)
4B1-18 Ni(0)
4B1-19
4B1-20 N-
B2 ES103
G
327
10101110 PC 100010101B2-08, 1B2-09, 1B2-10, 1B2-11,
1B2-121B2-08
1B2-09
1B2-10
1B2-11
1B2-12*
11201210 PC 111011201B2-15, 1B2-16, 1B2-17, 1B2-18,
1B2-191B2-15
1B2-16
1B2-17 -
1B2-18
1B2-19
327 14001450
PC 135014001B2-31, 1B2-32, 1B2-33, 1B2-34,1B2-35
1B2-31 B12-Ru
1B2-32
1B2-33
1B2-34
1B2-35 (EGB)
15001600 PC 145015001B2-37, 1B2-39, 1B2-40, 1B2-41,
1B2-421B2-37*
1B2-39 /Ti
1B2-40 Reductive acylation of phenylacetylene derivatives accompanying withtransposition of the triple bondNagaoka Univ. of Tech.ZHANG,Tianyuan; TAKANO, Atsushi; NISHIYAMA, Yutaro; MAEKAWA,
-
31
Hirofumi
1B2-41
1B2-42
328 10101110
PC 100010102B2-08, 2B2-09, 2B2-10, 2B2-11,2B2-12, 2B2-13
2B2-08
2B2-09
2B2-10 2,3--5,6--p-ALCA, JST
2B2-11 Mg/Me3SiCl/DMI
2B2-12 HFIP KF
2B2-13
11201220 PC 111011202B2-15, 2B2-17, 2B2-18, 2B2-19,
2B2-202B2-15* Fabrication of 3D Gradient Polymer Brush Based on BipolarElectrochemistryInterdisciplinary Grad. Sch. Sci. and Eng., Tokyo TechSHIDA, Naoki; FUCHIGAMI, Toshio; TOMITA, Ikuyoshi; INAGI,
Shinsuke
2B2-17 [18]
2B2-18
2B2-19 2,3--5,6--p-ALCA,JST
2B2-20
B3 ESES021
E
327
Si, Mn
910 1000 PC 9009101B3-02, 1B3-03, 1B3-04, 1B3-05,
1B3-061B3-02 1,3,6,8-
1B3-03 -
1B3-04 WPI-ITbMJST ERATO
1B3-05 2-
1B3-06 Endo-Mode Ring Closing Metathesis in Cp Manganese ComplexGrad. Sch. Sci., Osaka Pref. Univ.; CRC, Hokkaido Univ.TSENG, Ya-yi;KAMIKAWA, Ken; TAKAHASHI, Tamotsu; OGASAWARA, Masamichi
Cr, Re
10101110 PC 100010101B3-08, 1B3-10, 1B3-12, 1B3-131B3-08* Catalytic Enantioselective Synthesis of Planar-Chiral (-Arene)chromium Complexes by Mo-Catalyzed Ring-Closing MetathesisCRC,
Hokkaido Univ.; Grad. Sch. Sci., Osaka Pref. Univ.WU, Wei-yi; TSENG,Ya-yi; ARAE, Sachie; NAKAMURA, Chihiro; MORITA, Tomotaka;
TAKAHASHI, Tamotsu; OGASAWARA, Masamichi; KAMIKAWA, Ken
1B3-10* C-HCREST-JST
1B3-12 C(sp3)-H
1B3-13 --
Re, Ru
11201220 PC 111011201B3-15, 1B3-16, 1B3-17, 1B3-18,
1B3-19, 1B3-201B3-15 Markovnikov
1B3-16
1B3-17
1B3-18 /
1B3-19
1B3-20 /
327
Ru
13401440 PC 133013401B3-29, 1B3-30, 1B3-31, 1B3-32,
1B3-33, 1B3-341B3-29 Ru()-Pheox-Chanthamath Soda
1B3-30 -
1B3-31 7-
1B3-32 C-C
1B3-33
1B3-34
17001800 PC 165017001B3-49, 1B3-51, 1B3-52, 1B3-531B3-49*
1B3-51
1B3-52
1B3-53* Syntheses and Reactivities of Hydrido Carbonyl Ruthenium Com-plexes Bearing Various TriarylphosphinesFac. Sci. Tech., Keio Univ.OGIWARA, Yohei; KOCHI, Takuya; KAKIUCHI, Fumitoshi
328
Au
920 1010 PC 9109202B3-03, 2B3-04, 2B3-05, 2B3-06,
2B3-072B3-03
-
32
2B3-04 Nanoporous gold as a highly active catalyst for aerobic oxidation ofhydroxylamines into nitronesGrad. Sch. Sci., Tohoku Univ.KUSUMA,Indra; YUDHA, Salprima; ASAO, Naoki
2B3-05
Ag
2B3-06
Ni
2B3-07 Ni() N-
10201110 PC 101010202B3-09, 2B3-10, 2B3-11, 2B3-12,
2B3-132B3-09
2B3-10 3
2B3-11
2B3-12
2B3-13
Co
11201220 PC 111011202B3-15, 2B3-16, 2B3-17, 2B3-182B3-15 N-
2B3-16 o
2B3-17
2B3-18 Development of Cobalt-Catalyzed C-H BondFunctionalization ReactionsNanyang Tech. Univ.YOSHIKAI, Naohiko
328
Pt
13301430 PC 132013302B3-28, 2B3-29, 2B3-30, 2B3-31,
2B3-32, 2B3-332B3-28 PSiN--
2B3-29 (II)
2B3-30
Rh
2B3-31 - 1,6-[3.1.0]
2B3-32 (III)
2B3-33 (I) 1,2-2-
14401540 PC 143014402B3-35, 2B3-36, 2B3-37, 2B3-38,
2B3-39, 2B3-402B3-35 2,3-/
2B3-36 3--1,2-
2B3-37 [2+2+2]
2B3-38 ,-[2+2+2]
2B3-39 5-[2+2+2]
2B3-40
15501650 PC 154015502B3-42, 2B3-43, 2B3-44, 2B3-45,
2B3-46, 2B3-472B3-42 -5(4H)-
2B3-43 [2+2+2]
2B3-44 C-H
2B3-45
2B3-46 CO-C
2B3-47
17001730 PC 165017002B3-49, 2B3-50, 2B3-512B3-49
2B3-50
2B3-51 3-
329
Ti, Nb
900 1000 PC 8509003B3-01, 3B3-02, 3B3-03, 3B3-04,
3B3-05, 3B3-063B3-01
3B3-02
3B3-03
3B3-04 NbCl5
3B3-05
3B3-06 Nb
V, Bi, Te, Ga
10101110 PC 100010103B3-08, 3B3-09, 3B3-10, 3B3-11,
3B3-12, 3B3-133B3-08 5
3B3-09 (V)JST
3B3-10
3B3-11
3B3-12
3B3-13 Three-component Reaction of Esters with Silyl Cyanide and KeteneSilyl Acetals Catalyzed by Gallium TrihalidesGrad. Sch. Eng., Osaka
-
33
Univ.INAMOTO, Yoshihiro; KAGA, Yuta; NISHIMOTO, Yoshihiro;YASUDA, Makoto; BABA, Akio
In
11201220 PC 111011203B3-15, 3B3-16, 3B3-17, 3B3-18,
3B3-19, 3B3-203B3-15 -[2+2]
3B3-16
3B3-17
3B3-18
3B3-19 -
3B3-20
329
Rh
13301430 PC 132013303B3-28, 3B3-29, 3B3-30, 3B3-31,
3B3-32, 3B3-333B3-28 (III)[2 + 2 + 2]
3B3-29
3B3-30 Rh(I)-Catalyzed Arylative Double-Carbonylation of Alkynes withArylboronic Acids Using Formaldehyde as a CO SourceGrad. Sch. Mat.Sci., NAISTMORIMOTO, Tsumoru; WANG, Chuang; KAKIUCHI,Kiyomi; ARTOK, Levent
3B3-31
3B3-32 3
3B3-33 --,-
14401540 PC 143014403B3-35, 3B3-37, 3B3-38, 3B3-393B3-35*
3B3-37 1,2
3B3-38 sp2sp3
3B3-39*
15501650 PC 154015503B3-42, 3B3-43, 3B3-44, 3B3-45,
3B3-46, 3B3-473B3-42 N---
3B3-43 ,- 2,3-
3B3-44 2,5-
3B3-45 1--3-(2-)
3B3-46 3-
3B3-47
17001740 PC 165017003B3-49, 3B3-50, 3B3-51, 3B3-523B3-49
3B3-50
3B3-51 Ge-H C-H
3B3-52
330
Sr
910 1000 PC 9009104B3-02, 4B3-03, 4B3-04, 4B3-05,
4B3-064B3-02
4B3-03 Grignard
4B3-04
Ba
4B3-05 -
Y
4B3-06 4
Sc
10101110 PC 100010104B3-08, 4B3-10, 4B3-12, 4B3-134B3-08* Sc(OTf)3
4B3-10* Scandium-Catalyzed Enantioselective C-H Alkylation of PyridinesRIKEN Organometallic Chemistry LabSONG, Guoyong; HOU,Zhaomin
Sn
4B3-12
4B3-13
B4 ESES022
E
327
Pd
900 1000 PC 8509001B4-01, 1B4-03, 1B4-04, 1B4-051B4-01* Palladium-catalyzed One-shot Aromatic -Extension of PolycyclicAromatic HydrocarbonsGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTOZAKI, Kyohei; KAWASUMI, Katsuaki; ITO,Hideto; ITAMI, Kenichiro
1B4-03 2- C-H C-NWPI-ITbMJST ERATO
1B4-04 1,n-/
1B4-05* Synthesis of Cyclic Compounds by Cycloisomerization of Various 1,n-Dienes via Chain WalkingFac. Sci. Tech., Keio Univ.HAMASAKI, Taro;KAKIUCHI, Fumitoshi; KOCHI, Takuya
-
34
10101110 PC 100010101B4-08, 1B4-09, 1B4-11, 1B4-131B4-08 C-H/C-HERATO-JST
1B4-09* -
1B4-11* -
1B4-13 C-
11201220 PC 111011201B4-15, 1B4-16, 1B4-18, 1B4-201B4-15
1B4-16* Palladium-Catalyzed Regioselective C-H Fluorosilylation of 2-Phe-nylpyridines: Synthesis of Silafluorene EquivalentsGrad. Sch. Pharm., TheUniv. of Tokyo; The Univ. of Tokyo ERATO-JSTXIAO, Qing; MENG,Xiangtai; KANAI, Motomu; KUNINOBU, Yoichiro
1B4-18* Palladium-catalyzed Silylation and Germanylation of C(sp2)-H and C(sp3)-H BondsGrad. Sch. Pharm., The Univ. of TokyoKANYIVA,Stephen-kyalo; KUNINOBU, Yoichiro; KANAI, Motomu
1B4-20 [1,2-b:8,7-b]JSTACT-C
327
Rh
13401440 PC 133013401B4-29, 1B4-321B4-29
Pd
1B4-32
17001800 PC 165017001B4-49, 1B4-50, 1B4-51, 1B4-52,
1B4-53, 1B4-541B4-49 Pd 1
1B4-50
1B4-51
1B4-52 Pd
1B4-53
1B4-54 C-H 5
328
Ir
900 1000 PC 8509002B4-01, 2B4-02, 2B4-03, 2B4-04,
2B4-05, 2B4-062B4-01 1,3-
2B4-02 - 1,3-
2B4-03
2B4-04 C-H 1,3-[3 + 2]
2B4-05 C-H[3 + 2]
2B4-06
10101110 PC 100010102B4-08, 2B4-09, 2B4-10, 2B4-12,
2B4-132B4-08 C-H
2B4-09 C-H
2B4-10* /Me-BIPAM-
2B4-12 Synthesis of Triarylboranes via Iridium-Catalyzed C-H BorylationGrad. Fac. Eng., Hokkaido Univ.SASAKI, Ikuo; ISHIYAMA, Tatsuo;ITOU, Hajime
2B4-13 C-H WPI-ITbMJST ERATO
11201220 PC 111011202B4-15, 2B4-16, 2B4-182B4-15 Ir(III)-PNP
2B4-16* Syntheisis and Catalytic Function of Hydroxycyclopentadienyl Iri-dium ComplexGrad. Sch. Eng., The Univ. of TokyoKUSUMOTO,Shuhei; AKIYAMA, Midori; NOZAKI, Kyoko
2B4-18
328
Pd
13301430 PC 132013302B4-28, 2B4-30, 2B4-31, 2B4-32,
2B4-332B4-28* Modular Synthesis of Triarylmethanes through Palladium-CatalyzedSequential Arylation of Methyl Phenyl SulfoneWPI-ITbM, Nagoya Univ.NAMBO, Masakazu; CRUDDEN, Cathleen M.
2B4-30 -
2B4-31 Pd--
2B4-32 Synthetic Applications of-(Acylamino)alkylboronic Esters: Controlof Stereochemical Course in Catalytic Construction of Stereogenic Carbon
CentersGrad. Sch. Eng., Kyoto Univ.OHMURA, Toshimichi; MIWA,Kyoko; SUGINOME, Michinori
2B4-33 C1
14401540 PC 143014402B4-35, 2B4-36, 2B4-37, 2B4-38,
2B4-39, 2B4-402B4-35
2B4-36 -
2B4-37 NHC/Pd 2-2-
2B4-38 Pd 2-
2B4-39 PdWPI-AIMR
2B4-40 NHC -
15501650 PC 154015502B4-42, 2B4-43, 2B4-44, 2B4-45,
2B4-46, 2B4-472B4-42
-
35
2B4-43 HOMSi
2B4-44 - HOMSi
2B4-45
2B4-46 2- Pd
2B4-47
17001730 PC 165017002B4-49, 2B4-50, 2B4-512B4-49 Synthesis of Methoxy-Substituted Picenes and Eects of TheirPosition on Single Crystal StructuresGrad. Sch. Nat. Sci. Technol.,Okayama Univ.; Aichi Univ. of Educ. Dept. of Chem.; JST ACT-CCHEN, Xi-chao; CHANG, Ning-hui; MORI, Hiroki; NAKAJIMA, Kiyohiko;
NISHIHARA, Yasushi
2B4-50
2B4-51 Giese
329 900 1000
PC 8509003B4-01, 3B4-02, 3B4-03, 3B4-04,3B4-05, 3B4-06
3B4-01 DMF Pd 2,3-
3B4-02 -5(4H)-
3B4-03 An Improvement of Palladium Catalyst for the [4+2] Cycloadditionof o-(Silylmethyl)benzyl Carbonate with AlkenesFac. Sci., Kyushu Univ.JIN, Yushu; ISHIZUKA, Kentaro; KUWANO, Ryoichi
3B4-04
3B4-05
3B4-06
10101110 PC 100010103B4-08, 3B4-09, 3B4-10, 3B4-11,
3B4-12, 3B4-133B4-08
3B4-09
3B4-10 t-
3B4-11 SPRIX
3B4-12
3B4-13 FAN Lulu
11201220 PC 111011203B4-15, 3B4-16, 3B4-17, 3B4-193B4-15 Pd P-CP-
3B4-16 Pd 3
3B4-17* PQXphos
3B4-19* Quantication of steric inuence in palladium/alkylphosphine-sulfo-nate catalystsGrad. Sch. Eng., The Univ. of TokyoOTA, Yusuke; ITO,Shingo; NOZAKI, Kyoko
329
Pd, Ir
13301430 PC 132013303B4-28, 3B4-29, 3B4-30, 3B4-31,
3B4-323B4-28 31
3B4-29 3
3B4-30
3B4-31 Hydrothioalkylation of Electron-Decient Alkenes by PhotoredoxCatalysisChem. Res. Lab., Tokyo TechLI, Yanjie; MIYAZAWA, Kazuki;KOIKE, Takashi; AKITA, Munetaka
3B4-32* (HCOOH) MUCKERMAN James
Ir
14401540 PC 143014403B4-35, 3B4-36, 3B4-37, 3B4-38,
3B4-39, 3B4-403B4-35 Ir
3B4-36 2
3B4-37
3B4-38
3B4-39 C-H
3B4-40
15501650 PC 154015503B4-42, 3B4-43, 3B4-44, 3B4-45,
3B4-46, 3B4-473B4-42 Utility of a Trimethylsilyl Group as an Equivalent of HydroxylGroup: Synthesis of Alkanols via Iridium-Catalyzed C(sp3)-H Borylation
Grad. Sch. Eng., Kyoto Univ.OHMURA, Toshimichi; TORIGOE,Takeru; SUGINOME, Michinori
3B4-43
3B4-44
3B4-45 ,[2+2+2]
3B4-46
3B4-47
17001800 PC 165017003B4-49, 3B4-50, 3B4-51, 3B4-52,
3B4-53, 3B4-543B4-49 3 2 7 C-H
3B4-50 1 7-
3B4-51 C(sp3)-H
3B4-52 C-H
3B4-53
3B4-54 C-H-
-
36
330
Pd
900 1000 PC 8509004B4-01, 4B4-02, 4B4-03, 4B4-04,
4B4-054B4-01 Pd-Catalyzed Cascade Crossover Annulation of o-Alkynylarylhalidesand Diarylacetylenes Leading to Dibenzo[a,e]pentalenesWPI-AIMR,Tohoku Univ.ZHAO, Jian; ONIWA, Kazuaki; ASAO, Naoki;YAMAMOTO, Yoshinori; JIN, Tienan
4B4-02
4B4-03 2-
4B4-04 Enantioselective Palladium(II) Catalyzed Cyclization-CycloadditionCascade ReactionsISIR, Osaka Univ.ABOZEID , Mohamed;TAKIZAWA, Shinobu; SASAI, Hiroaki
4B4-05*
10101110 PC 100010104B4-08, 4B4-10, 4B4-11, 4B4-124B4-08* /
4B4-10 /
4B4-11 WPI-ITbMJST ERATO
4B4-12* o-- o-JSTACT-C
11201220 PC 111011204B4-15, 4B4-16, 4B4-17, 4B4-18,
4B4-19, 4B4-204B4-15 PCPPd
4B4-16
4B4-17
4B4-18
4B4-19 PGeP-Palladium Complex-Catalyzed Hydrocarboxylation of Alleneswith FormateGrad. Sch. Sci., Eng., Tokyo TechZHU, Chuan; SASANO,Kota; TAKAYA, Jun; IWASAWA, Nobuharu
4B4-20
B5 ESES024
D
327
900 1000 PC 8509001B5-01, 1B5-02, 1B5-03, 1B5-04,
1B5-05, 1B5-061B5-01 4
1B5-02 2 5--
1B5-03 1,14:7,8-Bis(dithio)-6,13-dithiopentacenequinone
1B5-04
1B5-05 D--A 1,4--1,3-
1B5-06
10101110 PC 100010101B5-08, 1B5-09, 1B5-10, 1B5-11,
1B5-12, 1B5-131B5-08 1B5-09
1B5-10 [4]
1B5-11 (5--2-)-1- 1,1-
1B5-12 2,4,6-(2-)-1,3,5-
1B5-13 (p-)
11201220 PC 111011201B5-15, 1B5-16, 1B5-17, 1B5-18,
1B5-19, 1B5-201B5-15 1-
1B5-16
1B5-17
1B5-18
1B5-19
1B5-20 1,3-
327 13301430
PC 132013301B5-28, 1B5-29, 1B5-30, 1B5-31,1B5-32, 1B5-33
1B5-28 Brnsted acid-catalyzed selective hydroboration of alkynylboronatesWPI-AIMR, Tohoku Univ.HO, Hon eong; ASAO, Naoki;YAMAMOTO, Yoshinori; JIN, Tienan
1B5-29 1B5-30
1B5-31 Rind(6)
1B5-32 diborane(4)
1B5-33
14401540 PC 143014401B5-35, 1B5-36, 1B5-37, 1B5-38,
1B5-39, 1B5-401B5-35
1B5-36 o-
1B5-37
1B5-38
1B5-39
1B5-40 Reaction of boryl metal species with dihydrogenGrad. Sch. Eng.,The Univ. of Tokyo; Fac. Sci. Eng., Chuo Univ.ARAMAKI, Yoshitaka;ZHAO, Xiaoxi; YAMASHITA, Makoto; NOZAKI, Kyoko
15501650 PC 154015501B5-42, 1B5-43, 1B5-44, 1B5-45,
1B5-46, 1B5-471B5-42
1B5-43
-
37
1B5-44 2,4,6--t- CH
1B5-45 -
1B5-46
1B5-47
17001750 PC 165017001B5-49, 1B5-50, 1B5-51, 1B5-52,
1B5-531B5-49 2- 2-
1B5-50
1B5-51 One-Pot
1B5-52
1B5-53
328 900 1000
PC 8509002B5-01, 2B5-02, 2B5-03, 2B5-04,2B5-05, 2B5-06
2B5-01
2B5-02 5
2B5-03 5
2B5-04
2B5-05 4,8-[1,2-d:4,5-d][1,2,3]/
2B5-06
10101110 PC 100010102B5-08, 2B5-09, 2B5-10, 2B5-11,
2B5-12, 2B5-132B5-08 [7]
2B5-09 : Wagner-Meerwein
2B5-10 12
2B5-11 buta-1,3-diy-nylbenzene
2B5-12
2B5-13 S-
11201220 PC 111011202B5-15, 2B5-16, 2B5-17, 2B5-18,
2B5-19, 2B5-202B5-15
2B5-16 BowlN-
2B5-17 Bowl
2B5-18 Ch(IV)=C=S(VI) (Ch = S, Se)
2B5-19
2B5-20
328 13301430
PC 132013302B5-28, 2B5-29, 2B5-30, 2B5-31,2B5-32, 2B5-33
2B5-28
2B5-29 2-(R)-(+)-
2B5-30 Pd/C
2B5-31 trans--
2B5-32
2B5-33
14401540 PC 143014402B5-35, 2B5-36, 2B5-37, 2B5-38,
2B5-39, 2B5-402B5-35
2B5-36 1--1,3- Diels-Alder
2B5-37 Rind
2B5-38 [3] 6
2B5-39
2B5-40 3
15501640 PC 154015502B5-42, 2B5-43, 2B5-44, 2B5-45,
2B5-462B5-42 8
2B5-43
2B5-44
2B5-45 JST-ERATO
2B5-46 9-
16501730 PC 164016502B5-48, 2B5-49, 2B5-50, 2B5-512B5-48 Wittig
2B5-49 6 Ph6Te
2B5-50 6
2B5-51 6 AIM
329 13201350
PC 131013203B5-27, 3B5-28, 3B5-293B5-27 1- 4,7-[b]
3B5-28
3B5-29 [2.2.2]
14001440 PC 135014003B5-31, 3B5-32, 3B5-333B5-31
3B5-32
-
38
3B5-33*
16501730 PC 164016503B5-48, 3B5-503B5-48* Ni / B(C6F5)3 Catalyst System for Highly Selective Crossed-Esterication of Triuoromethylketones with AldehydesGrad. Sch. Eng.,Osaka Univ.DOI, Ryohei; OHASHI, Masato; OGOSHI, Sensuke
3B5-50*
17401820 PC 173017403B5-53, 3B5-553B5-53* 1--1,3-
3B5-55* Synthetic Studies on Organoselenium-substituted Phosphenium Ca-tionsICR, Kyoto Univ.SUGAMATA, Koh; VILLALBA FRANCO, Josemanuel; SASAMORI, Takahiro; TOKITOH, Norihiro
B6 ESES025
A
327
900 1000 PC 8509001B6-01, 1B6-02, 1B6-03, 1B6-04,
1B6-05, 1B6-061B6-01 1,3- aza Diels-Alder
1B6-02 hetero Diels-Alder
1B6-03 2--
1B6-04 1 2 3,3-
1B6-05 -Pictet-SpenglerPark JiHyun
1B6-06 Friedel-Crafts
10101110 PC 100010101B6-08, 1B6-09, 1B6-10, 1B6-11,
1B6-12, 1B6-131B6-08 MannichRAHAMAN Hasibur
1B6-09
1B6-10 -
1B6-11 NicholasLI Feng
1B6-12
1B6-13 Mannich
11201220 PC 111011201B6-15, 1B6-16, 1B6-17, 1B6-19,
1B6-201B6-15 3,3--1,1--2,2-
1B6-16
1B6-17*
1B6-19
1B6-20
327 13301430
PC 132013301B6-28, 1B6-30, 1B6-31, 1B6-32,1B6-33
1B6-28* Copolymerization of carbon dioxide and dienes via lactone inter-mediateGrad. Sch. Eng., The Univ. of TokyoNAKANO, Ryo; ITO,Shingo; NOZAKI, Kyoko
1B6-30 1
1B6-31 2
1B6-32 YOOWoo-Jin
1B6-33 An Ecient Synthesis of Isocoumarins via N-Heterocyclic Carbene-Copper Complex Catalyzed Three-Component Coupling Reactions of Ben-
zynes, Terminal Alkynes, and Carbon DioxideGrad. Sch. Sci., The Univ. ofTokyoNGUYEN VU QUANG, Thanh; YOO, Woo-Jin; KOBAYASHI,Shu
14401540 PC 143014401B6-35, 1B6-37, 1B6-38, 1B6-39,
1B6-401B6-35* -
1B6-37 ,-(II)
-
39
1B6-38 FooSiong Wan
1B6-39 JST
1B6-40 1- SmI2 Zn
15501650 PC 154015501B6-42, 1B6-43, 1B6-44, 1B6-45,
1B6-46, 1B6-471B6-42 - (E)--[3+2]: Lectard Sylvain
1B6-43
1B6-44 //
1B6-45 SOD
1B6-46 (I)-
1B6-47 CH I2CNER
17001800 PC 165017001B6-49, 1B6-51, 1B6-52, 1B6-53,
1B6-541B6-49* Catalytic Hydrogenation of Carboxamides Using Ru ComplexBearing Tetradentate LigandGrad. Sch. Sci., Nagoya Univ.MIURA,Takashi; NARUTO, Masayuki; NOYORI, Ryoji; SAITO, Susumu
1B6-51
1B6-52
1B6-53
1B6-54
18101850 PC 180018101B6-56, 1B6-57, 1B6-581B6-56 //
1B6-57
1B6-58* --,-
328 900 1000
PC 8509002B6-01, 2B6-02, 2B6-03, 2B6-04,2B6-05
2B6-01
2B6-02 - Friedel-Crafts
2B6-03 C1- DielsAlder
2B6-04 Diels-Alder
2B6-05* - Diels-Alder
10101110 PC 100010102B6-08, 2B6-09, 2B6-10, 2B6-11,
2B6-132B6-08
2B6-09 1,3-
2B6-10
2B6-11* Petasis-FerrierGRIDNEV Ilya
2B6-13
11201220 PC 111011202B6-15, 2B6-17, 2B6-18, 2B6-19,
2B6-202B6-15* Site-Selective Aerobic Oxygenation of sp3 C-H Bonds of AlcoholsCovalently Bound to N-Oxyl Radical ActivatorGrad. Sch. Pharm., TheUniv. of TokyoOISAKI, Kounosuke; OZAWA, Jun; NI, Jizhi; TASHIRO,Masayuki; KANAI, Motomu
2B6-17
2B6-18 TMSNCS Nadaf Rashid Nabisaheb
2B6-19 1,5-
2B6-20
328 13301430
PC 132013302B6-28, 2B6-31, 2B6-32, 2B6-332B6-28 WPI-ITbM
2B6-31 Diels-Alder
2B6-32 Phase-transfer catalyzed asymmetric synthesis of 5,5-disubstitutedunsaturated -lactamsGrad. Sch. Sci., Kyoto Univ.ARLT, Alexander;HASHIMOTO, Takuya; MARUOKA, Keiji
2B6-33
14401540 PC 143014402B6-35, 2B6-37, 2B6-38, 2B6-392B6-35* N
2B6-37 2WPI-ITbMJST CREST
2B6-38 1,6- WPI-ITbMJST CREST
2B6-39* WPI-ITbMJST CREST
15501650 PC 154015502B6-42, 2B6-44, 2B6-45, 2B6-46,
2B6-472B6-42* 1,2-- Diels-AlderJST CREST
2B6-44 -JST CREST
2B6-45 Boronic Acid-DMAP(O) Cooperative Catalysis for DehydrativeCondensation between Carboxylic Acids and AminesGrad. Sch. Eng.,Nagoya Univ.LU, Yanhui; ISHIHARA, Kazuaki
2B6-46 (II)
2B6-47 Asymmetric catalytic activity of quaternary ammonium salts ofcinchona alkaloid containing acetylenic moietyToyohashi Univ. of Tech.HASSAN, Md. mehadi; HARAGUCHI, Naoki; ITSUNO, Shiniti
-
40
17001730 PC 165017002B6-49, 2B6-512B6-49*
2B6-51
329 900 1000
PC 8509003B6-01, 3B6-02, 3B6-03, 3B6-04,3B6-05, 3B6-06
3B6-01 1,2,3- 2,2- WPI-ITbMJST CREST
3B6-02 3-WPI-ITbMJST CREST
3B6-03 WPI-ITbMJST CREST
3B6-04
3B6-05 Morita-Baylis-Hillman
3B6-06 Baylis-Hillman
10101110 PC 100010103B6-08, 3B6-09, 3B6-10, 3B6-11,
3B6-123B6-08 3B6-09
3B6-10 /PPY:
3B6-11 MacMillan
3B6-12* Development of Catalytic Imine-imine Cross Coupling ReactionsGrad. Sch. Sci., The Univ. of TokyoMATSUMOTO, Masatoshi;HARADA, Masashi; YAMASHITA, Yasuhiro; KOBAYASHI, Shu
11201220 PC 111011203B6-15, 3B6-17, 3B6-18, 3B6-203B6-15* 3B6-17 -
3B6-18* N-Heterocyclic Carbene Catalyzed Umpolung of Michael AcceptorsNagoya Inst. of Tech. Department of Materials Science and EngineeringMATSUOKA, Shin-ichi; KATO, Terumasa; NAMERA, Shoko;
NAKAZAWA, Masanori; TAKAGI, Koji; SUZUKI, Masato
3B6-20 N-
329 16501740
PC 164016503B6-48, 3B6-49, 3B6-50, 3B6-51,3B6-52
3B6-48 Phospha-Brook--
3B6-49 Phospha-Brook
3B6-50 Lossen
3B6-51
3B6-52 -
17501830 PC 174017503B6-54, 3B6-55, 3B6-56, 3B6-573B6-54
3B6-55 - N- Claisen
3B6-56
3B6-57 HMPT CFBr3
ERATO-JST
B7 ESES033
A
327
900 1000 PC 8509001B7-01, 1B7-03, 1B7-04, 1B7-05,
1B7-061B7-01* -- 1,3-JST CREST
1B7-03 n-- Diels-AlderJST CREST
1B7-04
1B7-05 DielsAlder
1B7-06
10101110 PC 100010101B7-08, 1B7-10, 1B7-11, 1B7-12,
1B7-131B7-08*
1B7-10
1B7-11
1B7-12 2-
1B7-13
11201220 PC 111011201B7-15, 1B7-16, 1B7-17, 1B7-18,
1B7-19, 1B7-201B7-15
1B7-16
1B7-17 2,2,3-Trimethyl-2-silapent-4-ene
1B7-18 Felkin-Anh()
1B7-19 5-oxa-8-thiaspiro[3.4]oct-1-ene
1B7-20 Nazarov
327 13301430
PC 132013301B7-28, 1B7-29, 1B7-30, 1B7-31,1B7-33
1B7-28 -
1B7-29
1B7-30 JST CRESTUYANIK Muhammet
1B7-31* 2- JST CREST UYANIK
-
41
Muhammet1B7-33 JST CRESTUYANIKMuhammet
14401540 PC 143014401B7-35, 1B7-37, 1B7-38, 1B7-39,
1B7-401B7-35* ortho-/1,4-/ I2CNER
1B7-37 (III)ortho-JST CRESTUYANIK Muhammet
1B7-38 (III) 2,5-JST CRESTUYANIK Muhammet
1B7-39 (III) 1,5-
1B7-40 Baeyer-Villiger
UYANIK Muhammet15501650 PC 154015501B7-42, 1B7-43, 1B7-44, 1B7-45,
1B7-471B7-42 [3+2]
1B7-43 -
1B7-44
1B7-45* Dehydrogenation of primary alcohols using metal oxide photocata-lysts under visible light irradiationRCMS, Nagoya Univ.; Grad. Sch. Sci.,Nagoya Univ.; Inst. Adv. Res., Nagoya Univ.; Fac. Sci., Tokyo Univ. of Sci.NAKA, Hiroshi; LIU, Zijun; CANER, Joaquim; KUDO, Akihiko; NOYORI,
Ryoji; SAITO, Susumu
1B7-47
17001740 PC 165017001B7-49, 1B7-50, 1B7-51, 1B7-521B7-49 Visible Light-Mediated Chan-Lam Coupling Reactions of Arylboro-nic Acids and AminesGrad. Sch. Sci., The Univ. of TokyoYOO, Woo-Jin;TSUKAMOTO, Tatsuhiro; KOBAYASHI, Shu
1B7-50 YOO Woo-Jin
1B7-51
1B7-52
17501830 PC 174017501B7-54, 1B7-55, 1B7-56, 1B7-571B7-54 -
1B7-55 -
1B7-56 C-1 JACQUET AntoineROBERT FredericLANDAIS Yannick
1B7-57
328 900 1000
PC 8509002B7-01, 2B7-02, 2B7-03, 2B7-04,2B7-05, 2B7-06
2B7-01
2B7-02 YOO Woo-Jin
2B7-03
2B7-04 (V) Oxone
1 ,2-JSTCRESTUYANIK Muhammet
2B7-05 /JST CRESTUYANIK Muhammet
2B7-06 --JST CRESTUYANIK Muhammet
UYANIK Muhammet10101110 PC 100010102B7-08, 2B7-09, 2B7-10, 2B7-11,
2B7-12, 2B7-132B7-08
2B7-09 C(sp3)-H
2B7-10 1,3-
2B7-11 SmI2/Sm/Me3SiCl
2B7-12
2B7-13
11201210 PC 111011202B7-15, 2B7-16, 2B7-17, 2B7-18,
2B7-192B7-15 C-H/C-C
2B7-16 p-I-PhOH
2B7-17 BH3 SN2
2B7-18
2B7-19 WPI-AIMR
328 13301430
PC 132013302B7-28, 2B7-29, 2B7-30, 2B7-31,2B7-32, 2B7-33
2B7-28 LASC-SWNT
2B7-29 Lewis-(LASC)
2B7-30
2B7-31 (II)Mannich Diels-Alder
2B7-32 Diels-Alder
2B7-33 - 1,2- DielsAlderJST CREST
14401540 PC 143014402B7-35, 2B7-37, 2B7-38, 2B7-39,
2B7-402B7-35* Study of heterogeneous organic reactions using real-time reactionmonitoring with mass spectrometryGrad. Sch. Sci., The Univ. of TokyoMASUDA, Koichiro; KOBAYASHI, Shu
2B7-37
2B7-38 2,23 2,42
2B7-39 --,-
2B7-40 Lewis
-
42
15501650 PC 154015502B7-42, 2B7-43, 2B7-44, 2B7-46,
2B7-472B7-42 (II)
2B7-43 Cu(II) catalysis in asymmetric boron conjugate additions in organicsolventsGrad. Sch. Sci., The Univ. of TokyoZHU, Lei; KITANOSONO,Taku; XU, Pengyu; KOBAYASHI, Shu
2B7-44* Stereoselective synthesis of densely heterofunctionalized molecules bysecondary amine catalystsGrad. Sch. Sci., Kyoto Univ.SAKAMOTO,Ryu; KANO, Taichi; MARUOKA, Keiji
2B7-46 ,
2B7-47
17001730 PC 165017002B7-49, 2B7-50, 2B7-512B7-49
2B7-50 PyBidine aza-Henry
2B7-51 NHC,-
329 900 1000
PC 8509003B7-01, 3B7-02, 3B7-03, 3B7-04,3B7-05, 3B7-06
3B7-01 N-Mannich
3B7-02
3B7-03
3B7-04 /()
3B7-05
3B7-06 2-
10101110 PC 100010103B7-08, 3B7-09, 3B7-10, 3B7-11,
3B7-12, 3B7-133B7-08
3B7-09 1,4-
3B7-10 1,4-
3B7-11 2(3H)- antinitro-Michael
3B7-12
3B7-13 [2+2]
11201210 PC 111011203B7-15, 3B7-16, 3B7-17, 3B7-183B7-15 2-
3B7-16 - N-/Mi-chael
3B7-17 Michael
3B7-18* (III) 1,4-
329 17001740
PC 165017003B7-49, 3B7-50, 3B7-51, 3B7-523B7-49
3B7-50
3B7-51 (1,10)
3B7-52
17501830 PC 174017503B7-54, 3B7-55, 3B7-56, 3B7-573B7-54
3B7-55
3B7-56 Julia
3B7-57
B8 ESES034
A
327
900 1000 PC 8509001B8-01, 1B8-02, 1B8-03, 1B8-04,
1B8-051B8-01
1B8-02 1,2-JST ERATO
1B8-03
1B8-04
1B8-05* JST ERATO
10101110 PC 100010101B8-08, 1B8-09, 1B8-10, 1B8-11,
1B8-12, 1B8-131B8-08 Claisen CF3
1B8-09
1B8-10 redox
1B8-11 4,4,4--2--1-
1B8-12 1--1-
1B8-13 Gem-
11201220 PC 111011201B8-15, 1B8-16, 1B8-17, 1B8-18,
1B8-19, 1B8-201B8-15
1B8-16 (-)
-
43
1B8-17
1B8-18 sp3
1B8-19
1B8-20 2,3,3,3-
327 13301430
PC 132013301B8-28, 1B8-29, 1B8-30, 1B8-32,1B8-33
1B8-28 3,3-
1B8-29 C-F
1B8-30* HF
1B8-32 -
1B8-33
14401540 PC 143014401B8-35, 1B8-36, 1B8-37, 1B8-38,
1B8-39, 1B8-401B8-35
1B8-36 SN2-SNV
1B8-37 JST CREST
1B8-38 (III) 2-JST CREST
1B8-39
1B8-40
15501650 PC 154015501B8-42, 1B8-43, 1B8-451B8-42 -[3+2] 3-(-3-)-
1B8-43* Catalytic asymmetric [3+2] cycloaddition for indole compoundscontaining quaternary chiral carbon centerGrad. Sch. Sci., Chiba Univ.AWATA, Atsuko; ARAI, Takayoshi
1B8-45
17001740 PC 165017001B8-49, 1B8-51, 1B8-521B8-49* WPI-ITbMJST CREST
1B8-51 5-[3+2]WPI-ITbMJST CREST
1B8-52 -
17501830 PC 174017501B8-54, 1B8-55, 1B8-56, 1B8-571B8-54 redox C(sp3)-H
1B8-55 redox
1B8-56 redox
1B8-57 2,3--2,3--1,4-2,3--1,4-
328 900 1000
PC 8509002B8-01, 2B8-02, 2B8-03, 2B8-04,2B8-05, 2B8-06
2B8-01
2B8-02 3 H8-BINOL
2B8-03 3--H8-BINOL
2B8-04
2B8-05 -
2B8-06 -
10101110 PC 100010102B8-08, 2B8-10, 2B8-11, 2B8-12,
2B8-132B8-08* Development of Ecient Asymmetric [3+2] Cycloaddition ReactionsUsing Chiral Copper Amide CatalystsGrad. Sch. Sci., The Univ. of TokyoYOSHIMOTO, Susumu; YAMASHITA, Yasuhiro; KOBAYASHI, Shu
2B8-10 - Schiffendo [3+2]
2B8-11 /
2B8-12 -
2B8-13
11201220 PC 111011202B8-15, 2B8-16, 2B8-17, 2B8-18,
2B8-19, 2B8-202B8-15 2
2B8-16 -
2B8-17
2B8-18
2B8-19 HBr HBr
2B8-20 Henry
328 13301430
PC 132013302B8-28, 2B8-29, 2B8-30, 2B8-31,2B8-32, 2B8-33
2B8-28
2B8-29
2B8-30 Artocarpin
2B8-31 Valerenic acid
2B8-32
2B8-33 (+)-Duocarmycin A
14401540 PC 143014402B8-35, 2B8-36, 2B8-37, 2B8-38,
2B8-39, 2B8-402B8-35 19 D3A
2B8-36 ()
-
44
2B8-37
2B8-38
2B8-39 -
2B8-40
15501640 PC 154015502B8-42, 2B8-43, 2B8-44, 2B8-45,
2B8-462B8-42
2B8-43 O-Phosohinative Passerini/Pudovik : - one-pot
2B8-44 1Savukynas Vaidas
2B8-45 2
2B8-46 (E)-
16501730 PC 164016502B8-48, 2B8-49, 2B8-50, 2B8-512B8-48
2B8-49 6 3-[7]
2B8-50 16 3--5-[7]
2B8-51
329 900 1000
PC 8509003B8-01, 3B8-02, 3B8-03, 3B8-04,3B8-05, 3B8-06
3B8-01 - N-/
3B8-02 - N,N- N,N,C-
3B8-03
3B8-04
3B8-05 (II)
3B8-06
10101110 PC 100010103B8-08, 3B8-09, 3B8-10, 3B8-11,
3B8-123B8-08 (I)
3B8-09 ,---
3B8-10 3--2-
3B8-11 ,--- N-
3B8-12* ,- - N-
11201220 PC 111011203B8-15, 3B8-16, 3B8-17, 3B8-18,
3B8-203B8-15 Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxylate
3B8-16
3B8-17 1,2-E-WPI-ITbMJST CREST
3B8-18* WPI-ITbMJSTCREST
3B8-20 -
329 17001800
PC 165017003B8-49, 3B8-50, 3B8-52, 3B8-53,3B8-54
3B8-49 ---
3B8-50*
3B8-52 2-
3B8-53 ,
3B8-54 Enantioselective Organocatalyzed Synthesis of Cyclobutanes viaformal [2+2] CycloadditionISIR, Osaka Univ.ARTEAGA, Fernandoarteaga; TAKIZAWA, Shinobu; SASAI, Hiroaki
B9 ESES035
H
327
13001400 PC 125013001B9-25, 1B9-26, 1B9-27, 1B9-291B9-25 2,2,2--1-()
1B9-26
1B9-27*
1B9-29* Ecient amide bond formation through a rapid and strong activationof carboxylic acid, and its application for a synthesis of feglymycinGrad.Sch. Sci., Eng., Tokyo TechMIFUNE, Yuto; FUSE, Shinichiro; TANAKA,Hiroshi; TAKAHASHI, Takashi
14101510 PC 140014101B9-32, 1B9-34, 1B9-35, 1B9-36,
1B9-371B9-32* Multi-step Flow Synthesis of Optical Active -Amino Acid Deriva-tivesGrad. Sch. Sci., The Univ. of TokyoTSUBOGO, Tetsu;KOBAYASHI, Shu
1B9-34
1B9-35
1B9-36
1B9-37 -
15201620 PC 151015201B9-39, 1B9-40, 1B9-41, 1B9-43,
-
45
1B9-441B9-39
1B9-40 2-LeonardoDegennaroRenzo Luisi
1B9-41*
1B9-43
1B9-44 Hydrogenation of aromatic compounds using polysilane supportedrhodium/platinum nanoparticlesGrad. Sch. Sci., The Univ. of TokyoTAMMINANA, Ramana; YASUKAWA, Tomohiro; MIYAMURA,
Hiroyuki; KOBAYASHI, Shu
328 900 1000
PC 8509002B9-01, 2B9-02, 2B9-03, 2B9-04,2B9-05
2B9-01
2B9-02
2B9-03
2B9-04 Al-Sc
2B9-05* The Development of an Enzyme-Mimetic System with Catechol-Stabilized Naked Platinum Nanoclusters: Homogeneous Cooperative Catalysis
for Aerobic Oxidation of Amines to IminesGrad. Sch. Sci., The Univ. ofTokyoYUAN, Hao; MIYAMURA, Hiroyuki; KOBAYASHI, Shu
10101110 PC 100010102B9-08, 2B9-09, 2B9-10, 2B9-11,
2B9-12, 2B9-132B9-08 p
2B9-09 p
2B9-10 C-H 4
2B9-11
2B9-12 1,3,5-[(4-)]
2B9-13
11201200 PC 111011202B9-15, 2B9-17, 2B9-182B9-15* Development of asymmetric synthesis catalyzed by biomass supportedchiral rhodium nanoparticles and study of structureGrad. Sch. Sci., TheUniv. of TokyoYASUKAWA, Tomohiro; MIYAMURA, Hiroyuki;KOBAYASHI, Shu
2B9-17 Rh-
2B9-18 1,4-
329 900 1000
PC 8509003B9-01, 3B9-02, 3B9-03, 3B9-053B9-01
3B9-02
3B9-03*
3B9-05*
10101110 PC 100010103B9-08, 3B9-10, 3B9-11, 3B9-12,
3B9-133B9-08* The Eects of Amide Addition and Size of Nanoparticles in AerobicOxidation Reactions Catalyzed by Polymer Incarcerated Gold Nanoparticles
Grad. Sch. Sci., The Univ. of TokyoMIN, Hyemin; SOULE, Jean-Francois; MIYAMURA, Hiroyuki; KOBAYASHI, Shu
3B9-10 N-Alkylation of primary amides via hydrogen autotransfer facilitatedby metal nanoparticlesGrad. Sch. Sci., The Univ. of TokyoCHOO, ChongYu Gerald; MIYAMURA, Hiroyuki; KOBAYASHI, Shu
3B9-11 Aerobic oxidative aromatization catalyzed by polymer incarceratedgold nanoclusterGrad. Sch. Sci., The Univ. of TokyoMIYAMURA,Hiroyuki; KOBAYASHI, Shu
3B9-12
3B9-13
11201200 PC 111011203B9-15, 3B9-16, 3B9-17, 3B9-183B9-15 -
3B9-16
3B9-17 -DECHARIN Santida
3B9-18
C1 1 121
327
Fe
900 1000 PC 8509001C1-01, 1C1-02, 1C1-03, 1C1-04,
1C1-05, 1C1-061C1-01 -diketiminate
1C1-02
1C1-03 ALCA, JSTLEE YONG-MINNAM WONWOO
1C1-04
1C1-05 L-proline
1C1-06 (III)
Rh
10101110 PC 100010101C1-08, 1C1-09, 1C1-10, 1C1-121C1-08 JSTACT-C
1C1-09 Structures and Properties of Dinuclear Rhodium(I) Complexes withFormamidinato Bridging LigandsFac. Sci. Eng., Shimane Univ.; Sch. Sci.Tech., Kwansei Gakuin Univ.IDE, Yuki; IKEUE, Takahisa; INOUE,Ryoko; YOSHIOKA, Daisuke; MIKURIYA, Masahiro; HANDA, Makoto
1C1-10* CO
1C1-12*
-
46
Cr
11201200 PC 111011201C1-15, 1C1-17, 1C1-181C1-15* 2ALCA, JSTLIU ShuoBOUGHERCurtHICKS ScottABU-OMAR Mahdi M.
1C1-17 (V)-
1C1-18 (V)
328
Co,Rh,Ir
900 1010 PC 8509002C1-01, 2C1-02, 2C1-04, 2C1-05,
2C1-06, 2C1-072C1-01 B12
2C1-02* BadieiYosraMUCKERMAN James T.
2C1-04 C1 Rh
2C1-05 C-H
2C1-06
2C1-07 NCC
10201130 PC 101010202C1-09, 2C1-10, 2C1-11, 2C1-12,
2C1-13, 2C1-14, 2C1-152C1-09
2C1-10 HCl
2C1-11
2C1-12 SiNN
2C1-13 P-B-PIr
2C1-14 2
2C1-15
328
Co,Rh,Ir
14301530 PC 142014302C1-34, 2C1-35, 2C1-36, 2C1-37,
2C1-38, 2C1-392C1-34 PNP(I) C-H
2C1-35 Application of Bis(cyclometalated)iridium Complexes toward AlcoholOxidation and One-pot Dehydrogenative Silylation of Benzyl Alcohol
DerivativesSch. Eng. Sci., Osaka Univ.CHOI, Gyeongshin; TSURUGI,Hayato; MASHIMA, Kazushi
2C1-36 C-F
2C1-37 C-N
2C1-38 Ir-Vaska
2C1-39 8 9 N-H
15401640 PC 153015402C1-41, 2C1-42, 2C1-43, 2C1-44,
2C1-462C1-41 2C1-42 Cp*Rh(III) Cp*Ir(III) 1,4-
2C1-43 Ir(III)
2C1-44* Cp*Ir(III)
Ni,Pd,Pt
2C1-46
16501740 PC 164016502C1-48, 2C1-50, 2C1-51, 2C1-522C1-48*
2C1-50 Pd
2C1-51 Pd
2C1-52
329 900 1000
PC 8509003C1-01, 3C1-02, 3C1-03, 3C1-