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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.
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页码:1692 / 1695
页数:4
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