Photoinduced C(sp3)-H Chalcogenation of Amide Derivatives and Ethers via Ligand-to-Metal Charge-Transfer

被引:22
作者
Niu, Ben [1 ]
Sachidanandan, Krishnakumar [1 ]
Cooke, Maria Victoria [1 ]
Casey, Taylor E. [1 ]
Laulhe, Sebastien [1 ]
机构
[1] Indiana Univ Purdue Univ, Dept Chem & Chem Biol, Indianapolis, IN 46202 USA
关键词
VISIBLE-LIGHT; DIORGANYL DISELENIDES; IRON(III) CHLORIDE; ACTIVATION; CHEMISTRY; OXIDATION; ORGANOSELENIUM; RENAISSANCE; AMINATION; DIOXYGEN;
D O I
10.1021/acs.orglett.2c01505
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
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.
引用
收藏
页码:4524 / 4529
页数:6
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