Copper-Catalyzed Radical Reaction of N-Tosylhydrazones: Stereoselective Synthesis of (E)-Vinyl Sulfones

被引:83
|
作者
Mao, Shuai [1 ]
Gao, Ya-Ru [1 ]
Zhu, Xue-Qing [1 ]
Guo, Dong-Dong [1 ]
Wang, Yong-Qiang [1 ]
机构
[1] NW Univ Xian, Dept Chem & Mat Sci, Minist Educ, Key Lab Synthet & Nat Funct Mol Chem, Xian 710069, Peoples R China
基金
中国国家自然科学基金;
关键词
SULFINIC ACID SALTS; ALPHA-DIAZOCARBONYL COMPOUNDS; VINYL SULFONES; CARBONYL-COMPOUNDS; METAL CARBENE; CYCLOPROPANATION REACTIONS; 1,3-DIPOLAR CYCLOADDITION; BIOLOGICAL EVALUATION; MIGRATORY INSERTION; CONJUGATE ADDITION;
D O I
10.1021/acs.orglett.5b00461
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new chemistry of hydrazines that is a copper-catalyzed radical reaction to synthesize vinyl sulfones from readily available N-tosylhydrazones has been described. The protocol provides a novel strategy for the synthesis of various vinyl sulfones including alpha, beta-disubstituted ones and terminal ones. The advantages of the transformation include excellent E stereoselectivity, broad substrate scope, low cost of reagents, and convenient operation. A novel and efficient one-pot synthesis of alkynes from N-tosylhydrazones has been achieved. The studies provide important complementary approaches for the syntheses of vinyl sulfones and alkynes.
引用
收藏
页码:1692 / 1695
页数:4
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