Simple and convenient synthesis of 2-(substituted-benzylsulfanyl)-4,5-dihydrothiazoles and their antimicrobial activity studies
✍ Scribed by Ramanatham Vinod Kumar; Kotha V. S. R. Seshu Kumar
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 52 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
A simple and convenient procedure for the preparation of 2-(substitutedbenzylsulfanyl)-4,5-dihydrothiazoles by the reaction of 4,5-dihydro-thiazole-2-thiol and benzyl bromides in acetone/K 2 CO 3 condition has been reported.
📜 SIMILAR VOLUMES
## Abstract A number of new [(pyrazol‐4‐yl)methylene]hydrazono‐2,3‐dihydrothiazole derivatives, their sugar hydrazones and __N__‐glycosides were synthesized. Furthermore, __N__‐substituted oxygenated alkyl and hydroxyl derivatives and 1,3,4,‐oxadiazoline acyclic nucleoside analogs were prepared. Th
## Abstract The reaction of ethyl 4‐(benzofuran‐2‐yl)‐2,4‐dioxobutanoate **2** with two moles of hydrazine hydrate afforded 5‐(benzofuran‐2‐yl)‐1__H__‐pyrazole‐3‐carbohydrazide **4a**, while its reaction with equimolar amount of phenylhydrazine gave ester **3b** which then converted to 5‐(benzofura
## Abstract For Abstract see ChemInform Abstract in Full Text.