Simple and one-pot synthesis of new heterocyclic compounds in three-component reactions between isoquinoline or phenanthridine and acetylenic esters in the presence of n-heterocycles or 1,3-dicarbonyl compounds

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Abstract

A new class of enamino esters has been isolated in excellent yields from the 1:1:1 addition reaction between phenanthridine or isoquinoline and acetylenic esters such as ethyl propiolate or dialkyl acetylenedicaboxylates in the presence of heterocyclic NH compounds (succinimide, indole, 2-methylindole, 2-benzoxazolinone, 6-chlorobenzoxazolinone, carbazole and 3,6-dibromocarbazole) or 1,3-dicarbonyl compounds like 1,3-dimethylbarbituric acid, acetylacetone and dibenzoylmethane.

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Nassiri, M., Heydari, R., Hazeri, N., Habibi-Khorassani, S. M., Maghsoodlou, M. T., & Milani, F. J. (2010). Simple and one-pot synthesis of new heterocyclic compounds in three-component reactions between isoquinoline or phenanthridine and acetylenic esters in the presence of n-heterocycles or 1,3-dicarbonyl compounds. Arkivoc, 2010(2), 61–70. https://doi.org/10.3998/ark.5550190.0011.205

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