2010The Journal of Organic ChemistryRequires access

Asymmetric Direct Vinylogous Aldol Reaction of Unactivated γ-Butenolide to Aldehydes

Yang Yang, Ke Zheng, Jiannan Zhao, Jian Shi, Lili Lin, Xiaohua Liu, Xiaoming Feng

Open publisher page 65 citations

Abstract

The asymmetric direct vinylogous aldol reaction of unactivated gamma-butenolide with aldehydes has been developed, giving the corresponding 5-(1'-hydroxy)butenolide derivatives in high yields (up to 93%) and enantioselectivities (up to 83% ee) under mild conditions.

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What this paper is about

The asymmetric direct vinylogous aldol reaction of unactivated gamma-butenolide with aldehydes has been developed, giving the corresponding 5-(1'-hydroxy)butenolide derivatives in high yields (up to 93%) and enantioselectivities (up to 83% ee) under mild conditions.

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Available abstract

The asymmetric direct vinylogous aldol reaction of unactivated gamma-butenolide with aldehydes has been developed, giving the corresponding 5-(1'-hydroxy)butenolide derivatives in high yields (up to 93%) and enantioselectivities (up to 83% ee) under mild conditions.

Key concepts: Butenolide, Aldol reaction, Chemistry, Aldol condensation, Stereochemistry, Organic chemistry, Catalysis

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