Abstract
In the reaction of 1-cyano-2-naphthol (4) or its sodium salt with different alkylating agent, the O-alkylated derivatives (5a-d) were produced which underwent ring closure reactions using sodium ethoxide solution to give aminonaphtho [2,1-b]furan derivatives (6a-d). Ethyl 3-aminonaphtho[2,1-b]furan- 2-carboxylate (8) was reacted with formamide to afford naphtho[1′, 2′:4,5]furo[3,2-dlpyrimidine (11) derivatives. The produced pyrimidino compound underwent various reactions to synthesise other heterocyclic compounds.
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Badr, M. Z. A., El-Dean, A. M. K., Moustafa, O. S., & Zaki, R. M. (2006). Synthesis and biological study of some new naphtho[2,1-b]furan and related heterocyclic systems. Journal of Chemical Research, (11), 748–752. https://doi.org/10.3184/030823406779173433
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