Electron-transfer induced rearrangement of thiocyanate to isothiocyanate

…, T Etoh, H Yamamoto, S Yamamoto, Y Shigetomi

Index: Wakamatsu, Kan; Dairiki, Jun; Etoh, Tetsuo; Yamamoto, Hiroshi; Yamamoto, Satoshi; Shigetomi, Yasumasa Tetrahedron Letters, 2000 , vol. 41, # 3 p. 365 - 369

Full Text: HTML

Citation Number: 8

Abstract

Benzyl thiocyanates with an electron-withdrawing group (1a, 1b) and 9-fluorenyl thiocyanate (1e) rearrange to the corresponding isothiocyanate (2) under 9, 10-diphenylanthracene (DPA) sensitization. The rearrangement would proceed via carbon–sulfur bond cleavage ...

Related Articles:

Synthesis and cytotoxic evaluation of quinazolin-4 (3H)-one derivatives bearing thiocarbamate, thiourea or N-methyldithiocarbamate side chains

[Cao, Sheng-Li; Xu, Hong; Wang, Yao; Liao, Ji; Zhang, Jing-Jing; Li, Zhong-Feng; Guo, Yan-Wen; Li, Xiao-Rong; Cui, Xue-Mei; Xu, Xingzhi Medicinal Chemistry, 2012 , vol. 8, # 2 p. 163 - 173]

Structure–Activity Relationships (SAR) Research of Thiourea Derivatives as Dual Inhibitors Targeting both HIV??1 Capsid and Human Cyclophilin A

[Chen, Kan; Tan, Zhiwu; He, Meizi; Li, Jiebo; Tang, Shixing; Hewlett, Indira; Yu, Fei; Jin, Yinxue; Yang, Ming Chemical Biology and Drug Design, 2010 , vol. 76, # 1 p. 25 - 33]

Synthesis and octopaminergic agonist activity of 2-(substituted benzylamino)-2-thiazolines

[Hirashima, Akinori; Yoshii, Yutaka; Eto, Morifusa Bioscience, Biotechnology, and Biochemistry, 1992 , vol. 56, # 7 p. 1062 - 1065]

More Articles...