Highly Enantioselective Synthesis of α-Stereogenic Esters through Catalytic Asymmetric Michael Addition of 4-Oxo-4-arylbutenoates

ChemInform Abstract: Highly Enantioselective Synthesis of α-Stereogenic Esters Through Catalytic Asymmetric Michael Addition of 4-Oxo-4-arylbutenoates.

DFT study on two isomers of molecule C24H16: Two hexaprismanes linked by four carbon–carbon single bonds

The synthesis and photoluminescence of nanocrystalline Zr0.80Zn0.20O1.80+δ powders via glycine nitrate process

QS394. The Genomic Analysis of the Heterogeneity Hypoxia Responses in Renal Proximal Tubule Epithelial Cells After Knock-Down of HIF-1α and HIF-2α

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