Issue 19, 2016

E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition

Abstract

The stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition is reported. The reaction of silylketene acetals with N-tosylimines derived from β,γ-unsaturated α-keto esters in dichloromethane provided the corresponding (Z)-α,β-dehydroamino esters while the (E)-isomers were obtained when the reaction was carried out in the presence of 10 mol% copper(II) triflate.

Graphical abstract: E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition

Supplementary files

Article information

Article type
Communication
Submitted
21 Dec 2015
Accepted
31 Jan 2016
First published
01 Feb 2016

RSC Adv., 2016,6, 15655-15659

Author version available

E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition

M. Espinosa, A. García-Ortiz, G. Blay, L. Cardona, M. C. Muñoz and J. R. Pedro, RSC Adv., 2016, 6, 15655 DOI: 10.1039/C5RA27354D

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