z-logo
Premium
Sulfur nitride in organic chemistry. 6. Preparation of 3,4‐disubstituted 1,2,5‐thiadiazoles by the reaction of sulfur nitride with acetylenes
Author(s) -
Mataka Shuntaro,
Takahashi Kazufumi,
Yamada Yukihiro,
Tashiro Masashi
Publication year - 1979
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570160535
Subject(s) - chemistry , thiadiazoles , sulfur , nitride , organic chemistry , layer (electronics)
The reaction of sulfur nitride (1) with acetylenes (2a‐m) was carried out in refluxing toluene to give 1,2,5‐thiadiazoles (3a‐m) as a major product.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here