1999
DOI: 10.3987/com-99-8545
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Gould-Jacob Type of Reaction in the Synthesis of Thieno[3,2-e]pyrimido[1,2-c]pyrimidines: A Comparison of Classical Heating vs Solvent-Free Microwave Irradiation

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Cited by 20 publications
(11 citation statements)
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“…Dave et al obtained also thiopheno[3,2-e]pyrimido[1,2-c]pyrimidines (50)(Fig. 47)[181] and pyrido[3,2-e]pyrimidino[1,2-c]pyrimidines(51) …”
mentioning
confidence: 93%
“…Dave et al obtained also thiopheno[3,2-e]pyrimido[1,2-c]pyrimidines (50)(Fig. 47)[181] and pyrido[3,2-e]pyrimidino[1,2-c]pyrimidines(51) …”
mentioning
confidence: 93%
“…28 Yield, 85%, mp 181-183 • C; IR (KBr): ν = 2210 (CN), 1620, 1508 cm −1 (C C, C N ring); 1 H NMR (CDCl 3 ): δ = 1.…”
Section: -(3-chloro-4-fluorophenyl)-n-ethoxymethylene-2-amino-3-cyanmentioning
confidence: 99%
“…So far, there has not been any report on isomeric conversion in the pyrrolotriazolopyrimidine system. Therefore, in continuation of our interest in fused triheterocyclic pyrimidines [26][27][28][29], it was interesting to report the synthesis of 7H-pyrrolo [3,2- Therefore, in continuation of our interest in fused triheterocyclic pyrimidines [26][27][28][29], it was interesting to report the synthesis of 7H-pyrrolo [3,2- …”
Section: Introductionmentioning
confidence: 99%
“…73 . A one-pot synthesis of pyrano [2,3-d]pyrimidines was also described by Kidwai and co-workers starting from thiobarbituric acids.…”
Section: Fused Ring Heterocyclesmentioning
confidence: 99%