Reaction of N,N-disubstituted hydrazinecarbothioamides with 2-bromo-2-substituted acetophenones
| Autor: | Martin Nieger, El Shimaa S. M. AbdAl-Latif, Stephan Brase, Mahmoud A. A. Ibrahim, Alaa A. Hassan, Ashraf A. Aly |
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| Přispěvatelé: | Department of Chemistry |
| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
ETHYL
Chemistry & allied sciences 116 Chemical sciences Pyrazole 010402 general chemistry 01 natural sciences Medicinal chemistry lcsh:QD241-441 chemistry.chemical_compound lcsh:Organic chemistry ONE-POT REACTION Hydrazinecarbothioamides bis-thiazole MOIETIES AGENTS thiazoles 2-bromoacetophenones 010405 organic chemistry Chemistry DERIVATIVES Organic Chemistry SERIES 0104 chemical sciences 3. Good health pyrazole One pot reaction ddc:540 INHIBITORS |
| Zdroj: | ARKIVOC, Vol 2018, Iss 3, Pp 102-111 (2017) Arkivoc, 2018 (3), 102-111 |
| ISSN: | 1551-7012 1551-7004 |
| Popis: | Reaction of hydrazinecarbothioamides with 2-bromoacetophenones furnished the formation of thiazole-, bis-thiazole-, pyrazole- and 1,3,4-thiadiazole- derivatives in good yields. The mechanism was discussed. The structures of products were proved by MS, IR, NMR, elemental analyses and X-ray structure analyses. [GRAPHICS] . |
| Databáze: | OpenAIRE |
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