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Copper-Catalyzed Asymmetric Conjugate Additions of Bis(pinacolato)diboron and Dimethylzinc to Acyl- N-methylimidazole Michael Acceptors: A Highly Stereoselective Unified Strategy for 1,3,5,... n (OH, Me) Motif Synthesis.

作者信息

Lauberteaux Jimmy, Crévisy Christophe, Baslé Olivier, de Figueiredo Renata Marcia, Mauduit Marc, Campagne Jean-Marc

机构信息

Institut Charles Gerhardt Montpellier , UMR 5253 CNRS-UM-ENSCM, Ecole Nationale Supérieure de Chimie, Avenue Emile Jeanbrau , Montpellier 34296 Cedex 6 , France.

Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes , CNRS, ISCR UMR 6226, F-35000 Rennes , France.

出版信息

Org Lett. 2019 Mar 15;21(6):1872-1876. doi: 10.1021/acs.orglett.9b00479. Epub 2019 Feb 25.

Abstract

A unified strategy for the construction of prevalent 1,3,5,... n (OH, Me) motifs based on consecutive copper-catalyzed asymmetric conjugate borylation (ACB) and methylation (ACA) reactions involving α,β-unsaturated 2-acyl- N-methylimidazoles is described. Good yields and high diastereoselectivities have been obtained in ACA and ACB reactions for both matched and mismatched pairs as illustrated in the synthesis of syn/ anti and anti/ anti (Me, OTBS, Me) and (OH, OTBS, Me) motifs.

摘要

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