Synthesis of spiro-pyrazole-3,3′-thiopyrano[2,3-b]pyridines and azolo[a]pyrido[2′,3′:5,6]thiopyrano[3,4-d]pyrimidines as new ring systems with antifungal and antibacterial activities
✍ Scribed by Kamal M. Dawood
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 74 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Reactions
of 2,3-dihydro-4-oxo-thiopyrano[2,3-b]
pyridine with aldehydes and with DMF-DMA furnished the 3-benzylidene and 3-(N,N-dimethylamino)-methylene derivatives. The latter products afforded spiro-pyrazolo-3,3 '-thiopyrano[2,3-b]pyridines and new tetra-and penta-heterocyclic ring systems when treated with nitrilimines and aminoazoles, respectively. A number of the products showed high antifungal and antibacterial activities.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract The synthesis of new planar derivatives characterized by the presence of a pyridothiopyranopyrazole or pyridothiopyranopyrimidine nucleus, carrying a substituted aryl group, is reported. The novel 1,4‐dihydropyrido[3′,2′:5,6]thiopyrano[4,3‐__c__]pyrazole derivatives were obtained by con
## Abstract The synthesis of new pyrido[3′,2′:5,6]thiopyrano[3,2‐__b__]indol‐5(6__H__)‐ones was accomplished by the Fischer‐indole cyclization of some 2,3‐dihydro‐3‐phenylhydrazonothiopyrano[2,3‐__b__]pyridin‐4(4__H__)‐ones, obtained from the 2,3‐dihydro‐3‐hydroxymethylenethiopyrano[2,3‐__b__]pyrid
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