Issue 3, 2013

Organocatalytic asymmetric Michael reaction with acylsilane donors

Abstract

We have developed an organocatalytic asymmetric Michael reaction of acylsilane through the selection of acylsilane substrates and organocatalysts, thus creating a rare example of acylsilane α-alkylation with a chiral guanidine catalyst, which afforded products in good yields and high stereoselectivity. The corresponding adducts described here have also been demonstrated to be useful in the synthesis of unnatural amino acids and biologically active compounds.

Graphical abstract: Organocatalytic asymmetric Michael reaction with acylsilane donors

Supplementary files

Article information

Article type
Paper
Submitted
05 Oct 2012
Accepted
13 Nov 2012
First published
13 Nov 2012

Org. Biomol. Chem., 2013,11, 443-447

Organocatalytic asymmetric Michael reaction with acylsilane donors

L. Wu, G. Li, Q. Fu, L. Yu and Z. Tang, Org. Biomol. Chem., 2013, 11, 443 DOI: 10.1039/C2OB26950C

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