A leap forward in sulfonium salt and sulfur ylide chemistry

Author(s):  
Rong Fan ◽  
Chen Tan ◽  
Yongguo Liu ◽  
Yun Wei ◽  
Xiaowen Zhao ◽  
...  
Keyword(s):  
2006 ◽  
Vol 35 (1) ◽  
pp. 98-99 ◽  
Author(s):  
Yuichi Okazaki ◽  
Tatsuro Asai ◽  
Fumio Ando ◽  
Jugo Koketsu

Synthesis ◽  
2021 ◽  
Author(s):  
Qing-Zhu Li ◽  
Wen-Lin Zou ◽  
Zhi-Qiang Jia ◽  
Jun-Long Li

Allyl and propargyl sulfonium salts are readily available reagents and have recently emerged as versatile building blocks in the assembly of cyclic skeletons. As an alternative to the classical sulfonium salts, allyl and propargyl sulfonium salts can convert to 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 review, we provide a comprehensive overview of the recent developments on this growing field by summarizing the annulation reactions involving allyl and propargyl sulfonium salts.


ChemInform ◽  
2006 ◽  
Vol 37 (21) ◽  
Author(s):  
Yuichi Okazaki ◽  
Tatsuro Asai ◽  
Fumio Ando ◽  
Jugo Koketsu

1970 ◽  
Vol 35 (5) ◽  
pp. 1600-1604 ◽  
Author(s):  
Jerome. Adams ◽  
Lee. Hoffman ◽  
Barry M. Trost
Keyword(s):  

2021 ◽  
pp. 110525
Author(s):  
Shixiong Chen ◽  
Chun Cao ◽  
Xiaoming Shen ◽  
Yiwei Qiu ◽  
Cuifang Kuang ◽  
...  
Keyword(s):  

2014 ◽  
Vol 43 (9) ◽  
pp. 3424-3427
Author(s):  
D. E. Janzen ◽  
A. M. Kooyman

A trithiamacrocyclic ligand complex of Au(iii) undergoes a redox-mediated thermal reaction to form a chiral bicyclic sulfonium salt.


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