化学
酰胺
配体(生物化学)
金属
电荷(物理)
光化学
药物化学
立体化学
有机化学
受体
物理
生物化学
量子力学
作者
Ben Niu,Krishnakumar Sachidanandan,María Victoria Cooke,Taylor E. Casey,Sébastien Laulhé
出处
期刊:Organic Letters
[American Chemical Society]
日期:2022-06-21
卷期号:24 (25): 4524-4529
被引量:21
标识
DOI:10.1021/acs.orglett.2c01505
摘要
A photoinduced, iron(III) chloride-catalyzed C-H activation of N-methyl amides and ethers leads to the formation of C-S and C-Se bonds via a ligand-to-metal charge transfer (LMCT) process. This methodology converts secondary and tertiary amides, sulfonamides, and carbamates into the corresponding amido-N,S-acetal derivatives in good yields. Mechanistic work revealed that this transformation proceeds through a hydrogen atom transfer (HAT) involving chlorine radical intermediates.
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