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2000
Volume 23, Issue 23
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

An efficient and facial one-pot synthesis of 4-aryl-3,4-dihydrobenzo[g]quinoline- 2,5,10(1H)-triones was developed for the first time. The process proceeded via the three-component cyclocondensation of 2-amino-1,4-naphthoquinone with Meldrum’s acid and substituted benzaldehydes under green conditions. The fused 3,4-dihydropyridin-2(1H)- one-ring naphthoquinones have been synthesized with good to high yields in refluxing ethanol as a green reaction medium. This protocol is simple and effective as well as does not involve the assistance of the catalyst, additive, or hazardous solvents.

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/content/journals/coc/10.2174/1385272823666191108123330
2019-10-01
2025-01-15
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/content/journals/coc/10.2174/1385272823666191108123330
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