Regio- and Stereoselective Electro-Mediated Carboalkoxylation of 1,3-Dienes

IF 4.9 1区化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-12-16 DOI:10.1021/acs.orglett.4c03922

Ophélie Montiège, Marion Siccardi, Morgane Sanselme, Cédric Schneider, Jean-François Brière, Hélène Beucher

引用次数: 0

Abstract

1,3-Dienes are versatile raw materials for building molecular complexity. We report herein mild conditions for the regio- and stereoselective [only the (E) isomer obtained] 1,4-carboalkoxylation of 1,3-dienes. This electrochemical multicomponent reaction provides an eco-efficient and straightforward access to a diverse range of (E)-polyfunctionalized allyl ether products, without requiring any metal catalyst.

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1,3-Dienes 的区域和立体选择性电介导羰基氧合反应

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来源期刊

Organic Letters 化学-有机化学

CiteScore

9.30

自引率

11.50%

发文量

1607

审稿时长

1.5 months

期刊介绍： Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.

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