Palladium-catalyzed thiolation of alkanes and ethers with arylsulfonyl hydrazides

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.

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.


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

ChemInform ◽  
2015 ◽  
Vol 46 (33) ◽  
pp. no-no
Author(s):  
Ke Gao ◽  
Hideki Yorimitsu ◽  
Atsuhiro Osuka

2012 ◽  
Vol 134 (50) ◽  
pp. 20433-20439 ◽  
Author(s):  
Yoshinori Yamanoi ◽  
Junya Sendo ◽  
Tetsuhiro Kobayashi ◽  
Hiroaki Maeda ◽  
Yusuke Yabusaki ◽  
...  

2004 ◽  
Vol 69 (9) ◽  
pp. 3236-3239 ◽  
Author(s):  
Jungyeob Ham ◽  
Inho Yang ◽  
Heonjoong Kang

2015 ◽  
Vol 64 (5) ◽  
pp. 1065-1068
Author(s):  
O. V. Turova ◽  
V. G. Berezhnaya ◽  
E. V. Starodubtseva ◽  
M. G. Vinogradov

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