Ambient-Temperature Newman-Kwart Rearrangement Mediated by Organic Photoredox Catalysis

被引:66
作者
Perkowski, Andrew J. [1 ]
Cruz, Cole L. [1 ]
Nicewicz, David A. [1 ]
机构
[1] Univ N Carolina, Dept Chem, CB 3290, Chapel Hill, NC 27599 USA
关键词
ANTI-MARKOVNIKOV ADDITION; O-ARYL; SCHONBERG REARRANGEMENT; MICROWAVE SYNTHESIS; C-S; THIONCARBONATES; THIOPHENOLS; ANTAGONIST; CONVERSION; MECHANISM;
D O I
10.1021/jacs.5b11800
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Newman-Kwart rearrangement is perhaps the quintessential method for the synthesis of thiophenols from the corresponding phenol. However, the high thermal conditions required for the rearrangement of the requisite O-aryl carbamothioates often leads to decomposition. Herein, we present a general strategy for catalysis of O-aryl carbamothioates to S-aryl carbamothioates using catalytic quantities of a commercially available organic single-electron photooxidant. Importantly, this reaction is facilitated at ambient temperatures.
引用
收藏
页码:15684 / 15687
页数:4
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