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A Convenient Synthesis of 3,5-Diarylthieto[2,3-d]thiazole-2-thiones, and Expansion of Their Thiete Ring with Carbon Disulfide.

โœ Scribed by L. D. S. Yadav; Suman Dubey; Smita Singh


Publisher
John Wiley and Sons
Year
2010
Weight
29 KB
Volume
33
Category
Article
ISSN
0931-7597

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โœฆ Synopsis


Abstract

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๐Ÿ“œ SIMILAR VOLUMES


Reaction of 4-aryl-3-thiosemicarbazides
โœ Rafat M. Mohareb; Sherif M. Sherif ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 203 KB ๐Ÿ‘ 2 views

The reaction of 3-aryl-3-thiosemicarbazides 1a-d with carbon disulfide in alkaline medium affords the nonisolable sulfide salts 2a-d. The latter undergo in situ heterocyclization with some โฃ-halogenated compounds, e.g., 3a,b and 13, to afford polyfunctionally substituted 2,3-dihydrothiazoles 4a-e an