Phenanthridine or Isoquinoline are Good Reagents for the Synthesis of Enamino Esters
A new class of enamino esters has been isolated in excellent yields from the 1:1:1 addition reaction between phenanthridine or isoquinoline and activated acetylenic esters in the presence of heterocyclic NH compounds (succinimide, 5-nitroindazole, benzoxazolinone, 6-chlorobenzoxazolinone, carbazole...
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Veröffentlicht in: | Journal of chemical research 2010-07, Vol.34 (7), p.365-369 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new class of enamino esters has been isolated in excellent yields from the 1:1:1 addition reaction between phenanthridine or isoquinoline and activated acetylenic esters in the presence of heterocyclic NH compounds (succinimide, 5-nitroindazole, benzoxazolinone, 6-chlorobenzoxazolinone, carbazole and 3,6-dibromocabazole) or 1,3-dicarbonyl compounds such as 1,3-dimethylbarbituric acid and 1,3-diethyl-2-thiobar- bituric acid. |
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ISSN: | 1747-5198 2047-6507 |
DOI: | 10.3184/030823410X12767058123665 |