Reactions of aromatic sulphenyl compounds with organotin compounds
JL Wardell, S Ahmed
Index: Wardell,J.L.; Ahmed,S. Journal of Organometallic Chemistry, 1974 , vol. 78, p. 395 - 404
Full Text: HTML
Citation Number: 41
Abstract
Aromatic sulphenyl halides and thiocyanates, RSX, cleave aryltin bonds, ArSn , when the aryl groups contain strongly electron releasing substituents, to give monosulphides, RSAr. The reaction of o-NO 2 C 6 H 4 SCl and Ph 3 SnCHCH 2 gave both the cleavage product, CH 2 CHSC 6 H 4 NO 2 -o, and the addition product, Ph 3 SnCHClCH 2 SC 6 H 4 NO 2 -o. Other organotin bonds cleaved by o-NO 2 C 6 H 4 SCl are p-MeC 6 H 4 SCH 2 CH 2 Sn (to ...
Related Articles:
[Deng, Wei; Zou, Yan; Wang, Ye-Feng; Liu, Lei; Guo, Qing-Xiang Synlett, 2004 , # 7 p. 1254 - 1258]
[Duan, Zhongyu; Ranjit, Sadananda; Zhang, Pengfei; Liu, Xiaogang Chemistry - A European Journal, 2009 , vol. 15, # 15 p. 3666 - 3669]
[Duan, Zhongyu; Ranjit, Sadananda; Zhang, Pengfei; Liu, Xiaogang Chemistry - A European Journal, 2009 , vol. 15, # 15 p. 3666 - 3669]