Recent Advances on Annulation Reactions with Allyl and Propargyl Sulfonium Salts

被引:13
作者
Li, Qing-Zhu [1 ]
Zou, Wen-Lin [1 ]
Jia, Zhi-Qiang [1 ]
Li, Jun-Long [1 ]
机构
[1] Chengdu Univ, Sichuan Ind Inst Antibiot Sch Pharm, Antibiot Res & Re Evaluat Key Lab Sichuan Prov, Chengdu 610106, Peoples R China
来源
SYNTHESIS-STUTTGART | 2022年 / 54卷 / 01期
基金
中国国家自然科学基金;
关键词
allyl sulfonium salts; propargyl sulfonium salts; sulfur ylides; allenyl sulfonium salts; annulation reactions; SULFUR YLIDES; PROP-2-YNYLSULFONIUM SALTS; DIASTEREOSELECTIVE SYNTHESIS; REGIOSELECTIVE SYNTHESIS; CYCLIZATION REACTIONS; AZAOXYALLYL CATIONS; MICHAEL ADDITION; CYCLOPROPANATION; ACCESS; BENZANNULATION;
D O I
10.1055/a-1578-2911
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Allyl and propargyl sulfonium salts are readily available reagents that have recently emerged as versatile building blocks for the assembly of cyclic skeletons. As an alternative to classical sulfonium salts, allyl and propargyl sulfonium salts can be converted into the corresponding vinyl sulfur ylide or allenic sulfonium salt intermediates that contain diverse nucleophilic or electrophilic reactive positions, thereby enabling a great variety of annulation reactions. In this short review, we provide a comprehensive overview of the recent developments in this growing field by summarizing annulation reactions involving allyl and propargyl sulfonium salts. 1 Introduction 2 Annulations with Allyl Sulfonium Salts 3 Annulations with Propargyl Sulfonium Salts 4 Conclusion
引用
收藏
页码:67 / 78
页数:12
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