Reaction of trithiazyl trichloride with alkenes and alkynes

XG Duan, XL Duan, CW Rees, TY Yue

Index: Duan, Xiao-Guang; Duan, Xiao-Lan; Rees, Charles W.; Yue, Tai-Yuen Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 17 p. 2597 - 2601

Full Text: HTML

Citation Number: 19

Abstract

Alkenes and alkynes react readily with trithiazyl trichloride 1 to give 1, 2, 5-thiadiazoles 2 in one step. Thus 3-amino-1, 2, 5-thiadiazole 5 is now readily available from N- vinylphthalimide and 1 in two steps. Cyclic alkenes react similarly to give fused thiadiazoles (7, 12) and phenanthrene gives the phenanthrothiadiazole 16. Tetra-substituted alkenes such as 13 appear to give the analogous 3, 4-dihydrothiadiazoles (eg 14) which ...

Related Articles:

General synthetic system for 1, 2, 5-thiadiazoles

[Journal of Organic Chemistry, , vol. 32, p. 2823 - 2829]

The Preparation and Characterization of 5-Substituted-4-chloro-1, 2, 3-dithiazolium Salts and their Conversion into 4-Substituted-3-chloro-1, 2, 5-thiadiazoles

[Molecules, , vol. 10, # 2 p. 346 - 359]

More Articles...