Visible-light-induced iodine-anion-catalyzed decarboxylative/deaminative C–H alkylation of enamides

文献信息

发布日期 2021-06-07

DOI 10.1039/D1QO00660F

影响因子 5.281

作者

Jia-Xin Wang, Ya-Ting Wang, Hao Zhang, Ming-Chen Fu

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摘要

A visible-light-induced iodine-anion-catalyzed C–H stereoselective alkylation of enamides has been developed. Redox-active esters and Katritzky salts of amino acids were found to be amenable for decarboxylative/deaminative cross-coupling reactions, delivering various functionalized enamides with excellent functional group tolerance. The reaction proceeded via photoactivation of the transiently assembled chromophores, avoiding the use of exogenous precious photoredox catalysts.

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来源期刊

Organic Chemistry Frontiers

CiteScore: 7.8

自引率: 8.7%

年发文量: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Visible-light-induced iodine-anion-catalyzed decarboxylative/deaminative C–H alkylation of enamides

文献信息

期刊推荐

相关文献

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