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Ficini Reaction with Acrylates for the Stereoselective Synthesis of Aminocyclobutanes.

作者信息

Robert Emma G L, Waser Jerome

机构信息

Laboratory of Catalysis and Organic Synthesis, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LCSO, BCH 4306, 1015, Lausanne, Switzerland.

出版信息

Chemistry. 2024 Oct 17;30(58):e202401810. doi: 10.1002/chem.202401810. Epub 2024 Oct 2.

Abstract

The first Ficini reaction between ynamides and acrylates is reported herein. The reaction is catalyzed by B(CF) acting as a Lewis acid and is giving access to stable tri-substituted aminocyclobutenes in high yield. The resulting products can be hydrogenated and epimerized under basic conditions or in presence of a Lewis acid, providing two distinct trans- aminocyclobutane monoester stereoisomers in high yield and diastereoisomeric ratio (up to quantitative yield and >99 : 1 dr).

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