A New Method for the Preparation of Alkyl Aryl Sulfides from Alcohols via Alkoxydiphenylphosphines by Oxidation–Reduction Condensation

2004 ◽  
Vol 33 (11) ◽  
pp. 1522-1523 ◽  
Author(s):  
Teruaki Mukaiyama ◽  
Kazuhiro Ikegai
Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 986-992 ◽  
Author(s):  
M. Soleiman-Beigi ◽  
Z. Arzehgar

An efficient and new method for the synthesis of disulfides and sulfides via the reaction of aryl halides with ethyl potassium xanthogenate in the presence of MOF-199 is described. O-Ethyl-S-aryl ­carbonodithioate has a key role as an intermediate in this procedure; it was converted into symmetrical diaryl disulfides in DMF. Additionally, this could be applied to the synthesis of unsymmetrical aryl alkyl(aryl′) disulfides by the reaction with S-alkyl(aryl) sulfurothioates (Bunte salts) as well as unsymmetrical aryl alkyl(aryl′) sulfides in DMSO.


2014 ◽  
Vol 50 (62) ◽  
pp. 8578-8581 ◽  
Author(s):  
Sheng-rong Guo ◽  
Wei-ming He ◽  
Jian-nan Xiang ◽  
Yan-qin Yuan

A new method for the preparation of alkyl aryl sulfides through direct oxidative thiolation of alkanes or ethers with arylsulfonyl hydrazides using DTBP as an oxidant catalyzed by Pd(OAc)2 has been reported. The C–H bonds in various alkanes or ethers were successfully converted into C–S bonds with moderate to good yields.


1966 ◽  
Vol 39 (2) ◽  
pp. 411-411 ◽  
Author(s):  
Hiroshi Yoshida ◽  
Saburo Inokawa ◽  
Tsuyoshi Ogata
Keyword(s):  

2009 ◽  
Vol 82 (3) ◽  
pp. 381-392 ◽  
Author(s):  
Kiichi Kuroda ◽  
Yuji Maruyama ◽  
Yujiro Hayashi ◽  
Teruaki Mukaiyama

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