Journal
CHEMISTRY OF HETEROCYCLIC COMPOUNDS
Volume 44, Issue 12, Pages 1510-1519Publisher
SPRINGER
DOI: 10.1007/s10593-009-0217-7
Keywords
vinyl-substituted isoxazolopyrimidone; vinyl-substituted thiadiazolopyrimidone; vinyl-substituted thiazolopyrimidinone; triazolopyrimidoazocine; ring scission
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Funding
- RFFI [07-03-1209-ofi]
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It has been established that 5-vinyl-substituted (N-R,N-vinylaminomethyl)isoxazolo(thiazolo, thiadiazolo)pyrimidines are formed when tetrahydropyrido[3,4-d]pyrimidines, annelated with isoxazole, thiazole, and thiadiazole units are treated with terminal alkynes as a result of opening of the tetrahydropyridine ring. 7-Methoxymethyl-substituted [N-R,N-(dimethoxycarbonylvinyl)]aminoethyl-isoxazolo- and thiazolopyrimi-dines were obtained by reaction with dimethyl acetylenedicarboxylate (ADCE). Triazolo-pyrimidoazocine was obtained for the first time from tetrahydrotriazolopyrimidine and methyl propiolate.
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