Visible-light-induced iodine-anion-catalyzed decarboxylative/deaminative C–H alkylation of enamides
Literature Information
Publication Date
2021-06-07
DOI
10.1039/D1QO00660F
Impact Factor
5.281
Authors
Jia-Xin Wang, Ya-Ting Wang, Hao Zhang, Ming-Chen Fu
View Original
Abstract
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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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
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
Recommended Compounds
Methyl 2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oate
CAS Number:
218600-53-4
Molecular Formula:
C32H43NO4
![[4-Amino-2-(methylsulfanyl)-5-pyrimidinyl]methanol structure](https://static.chemtradehub.com/structs/588/588-36-3-fc73.webp "[4-Amino-2-(methylsulfanyl)-5-pyrimidinyl]methanol structure")
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