Cyclocondensation of β-enaminonitriles, carbonyl compounds and acetonitrile. An effective route to various six-membered lactams

P. Nemes, B. Balázs, G. Toth, P. Scheiber

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

A cyclocondensation of β-enaminonitriles, carbonyl compounds and acetonitrile is described. Using different cyclic or open chain enaminonitriles various N-heterocycles were obtained in a one-step procedure. The base catalysed reaction was also carried out with α,β-unsaturated nitriles under similar conditions.

Original languageEnglish
Pages (from-to)1327-1329
Number of pages3
JournalSynlett
Issue number9
Publication statusPublished - 2000

Fingerprint

Lactams
Carbonyl compounds
Nitriles
enaminonitrile
acetonitrile

Keywords

  • α,β-Unsaturated nitriles
  • β-Enaminonitriles
  • Alkaloid analogues
  • Cyclocondensation
  • Polycyclic lactams

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Cyclocondensation of β-enaminonitriles, carbonyl compounds and acetonitrile. An effective route to various six-membered lactams. / Nemes, P.; Balázs, B.; Toth, G.; Scheiber, P.

In: Synlett, No. 9, 2000, p. 1327-1329.

Research output: Contribution to journalArticle

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AU - Scheiber, P.

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