3H-1,2,4-Dithiazol-3-one compounds as novel potential affordable antitubercular agents
โ Scribed by Yang, Jianzhong; Pi, Weiyi; Xiong, Li; Ang, Wei; Yang, Tao; He, Jun; Liu, Yuanyuan; Chang, Ying; Ye, Weiwei; Wang, Zhenling; Luo, Youfu; Wei, Yuquan
- Book ID
- 123058494
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 295 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0960-894X
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๐ SIMILAR VOLUMES
A series of triazines have been synthesized starting from 5-alkyl-1,3,4-thiadiazole-2-thioles (1a-d). On reaction with ethyl bromoacetate in the presence of anhydrous K 2 CO 3 under microwave irradiation (MWI), these yielded corresponding esters (2a-d) which on hydrazinolysis under MWI produced (5-a
The reactivity of 5-amino-3H-1,2,4-dithiazole-3-thiones substituted at their amino group and 5-amino-3H-1,2-dithiole-3-thiones substituted at their amino group and C4 toward compounds containing P(III) atoms has been studied. N,N-Disubstituted-N 0 -(3-thioxo-3H-1,2,4-dithiazol-5-yl)methanimidamides