Forging C–S Bonds Through Decarbonylation New Perspectives for the Synthesis of Privileged Aryl Sulfides

ChemCatChem ◽  
2021 ◽  
Author(s):  
Chengwei Liu ◽  
Michal Szostak
Keyword(s):  
ChemInform ◽  
2015 ◽  
Vol 46 (33) ◽  
pp. no-no
Author(s):  
Ke Gao ◽  
Hideki Yorimitsu ◽  
Atsuhiro Osuka

2011 ◽  
Vol 76 (11) ◽  
pp. 4371-4378 ◽  
Author(s):  
Namjin Park ◽  
Kyungho Park ◽  
Mihee Jang ◽  
Sunwoo Lee

ChemInform ◽  
2013 ◽  
Vol 44 (40) ◽  
pp. no-no
Author(s):  
Michal Majek ◽  
Axel Jacobi von Wangelin
Keyword(s):  

2021 ◽  
Author(s):  
Navin Yadav ◽  
Soumen Payra ◽  
J. Narasimha Moorthy

The reaction between aryl olefins and thiols in the presence of Oxone in toluene-water (9:1, v/v) affords β-hydroxy-2-arylethyl aryl sulfides smoothly by interception of the intermediary thiyl radicals with aryl...


2010 ◽  
Vol 12 (10) ◽  
pp. 2430-2433 ◽  
Author(s):  
Zhongyu Duan ◽  
Sadananda Ranjit ◽  
Xiaogang Liu

2017 ◽  
Vol 4 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Yang Wang ◽  
Xiaofeng Zhang ◽  
Haixiong Liu ◽  
Hui Chen ◽  
Deguang Huang

Unsymmetrical aryl sulfides were synthesized by nickel-catalyzed arylsulfonyl chlorides and aryl iodides via intermediate disulfides using Mn as a reducing agent.


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