ChemInform Abstract: Organocatalytic Asymmetric “anti-Michael” Reaction of β-Ketoesters.
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2008 Enantioselective syntheses O 0031 Organocatalytic Asymmetric "anti-Michael" Reaction of β-Ketoesters. — The organocatalytic enantioselective anti-Michael addition uses a sulfone as directing group of the regioselectivity and as a leaving group in the same reaction. These prop- erties allow the creation of α,α'-branched terminal double bond joined to a quaternary center. — (ALEMAN, J.; REYES, E.; RICHTER, B.; OVERGAARD, J.; JOERGENSEN*, K. A.; Chem. Commun. (Cambridge) 2007, 38, 3921-3923; Dep. Chem., Univ. Aarhus, DK-8000 Aarhus, Den.; Eng.) — M. Paetzel 06- 028
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Transcript of ChemInform Abstract: Organocatalytic Asymmetric “anti-Michael” Reaction of β-Ketoesters.
2008
Enantioselective synthesesO 0031 Organocatalytic Asymmetric "anti-Michael" Reaction of β-Ketoesters. —
The organocatalytic enantioselective anti-Michael addition uses a sulfone as directing group of the regioselectivity and as a leaving group in the same reaction. These prop-erties allow the creation of α,α'-branched terminal double bond joined to a quaternary center. — (ALEMAN, J.; REYES, E.; RICHTER, B.; OVERGAARD, J.; JOERGENSEN*, K. A.; Chem. Commun. (Cambridge) 2007, 38, 3921-3923; Dep. Chem., Univ. Aarhus, DK-8000 Aarhus, Den.; Eng.) — M. Paetzel
06- 028