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Recent advances in thiolation via sulfur electrophiles
被引:49
|作者:
Wei, Ya-Feng
[1
]
Gao, Wen-Chao
[1
,2
]
Chang, Hong-Hong
[1
]
Jiang, Xuefeng
[2
]
机构:
[1] Taiyuan Univ Technol, Coll Biomed Engn, Taiyuan 030024, Peoples R China
[2] East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China
基金:
中国国家自然科学基金;
关键词:
BOND INSERTION REACTION;
C-H SULFENYLATION;
ENANTIOSELECTIVE SULFENYLATION;
INTRAMOLECULAR SULFENOAMINATION;
CATALYZED SULFENYLATION;
N-SULFANYLSUCCINIMIDES;
BETA-KETOESTERS;
SULFIDES;
ALKENES;
ARYL;
D O I:
10.1039/d2qo01447e
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Umpolung of thiols has become a common strategy for the synthesis of various S-containing compounds and thus a series of sulfur electrophiles have been designed and applied for diverse thiolations. To meet different demands for the incorporation of thio groups with regio- and stereoselectivity, new catalyst systems and methodologies based on the utility of sulfur electrophiles have been well developed. In this review, achievements on various thiolation methodologies with sulfur electrophiles have been summarized, mainly including thiofunctionalization of alkenes or alkynes, insertion of carbene precursors, C-S cross coupling and electrophilic substitution, aiming to give a comprehensive insight into the application of electrophilic sulfur reagents.
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页码:6684 / 6707
页数:24
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