Synthesis 2016; 48(19): 3413-3419
DOI: 10.1055/s-0035-1562785
paper
© Georg Thieme Verlag Stuttgart · New York

Highly Diastereoselective and Irreversible Aldol Reactions of N-Sulfonylimidates

Hannah E. Bartrum
a   Univ. Grenoble Alpes, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France
b   CNRS, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France   Email: jean-francois.poisson@univ-grenoble-alpes.fr
,
Sébastien Carret
a   Univ. Grenoble Alpes, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France
b   CNRS, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France   Email: jean-francois.poisson@univ-grenoble-alpes.fr
,
Jean-François Poisson*
a   Univ. Grenoble Alpes, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France
b   CNRS, Département de Chimie Moléculaire (DCM), 38000 Grenoble, France   Email: jean-francois.poisson@univ-grenoble-alpes.fr
› Author Affiliations
Further Information

Publication History

Received: 26 May 2016

Accepted after revision: 29 June 2016

Publication Date:
30 August 2016 (online)


Dedicated to the memory of Prof. Jean Normant, an exceptional and inspiring supervisor

Abstract

A mild method for the aldolization of N-sulfonylimidates was developed. The reaction proceeds in excellent diastereoselectivity to provide a range of useful β-hydroxyimidates in high yield. The innate reversibility of the reaction is suppressed by the use of a titanium complex as a Lewis acid.

Supporting Information

 
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