4.4 Article

A Baker-Venkataraman retro-Claisen cascade delivers a novel alkyl migration process for the synthesis of amides

期刊

TETRAHEDRON LETTERS
卷 56, 期 14, 页码 1816-1819

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2015.02.077

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Baker-Venkataraman; retro-Claisen; Rearrangement; Amide

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A simple extension of the carbamoyl Baker-Venkataraman rearrangement has been developed. If residual water in the reaction is not strictly excluded a Baker-Venkataraman retro-Claisen cascade takes place, giving amide products, in which an alkyl group apparently migrates between two functionalities of the substrate. (C) 2015 Elsevier Ltd. All rights reserved.

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