Synthesis and stereochemistry of azeto[2,1-a]isoquinolin-2-one derivatives

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Azeto[2,1-a]isoquinolin-2-one derivatives 3-7 were prepared by the reaction of dihydro-isoquinoline 1a or 1b with the corresponding acid chloride 2a-c in the presence of triethylamine. Alternatively, 4 was obtained by the reaction of 1a and phenoxyacetic acid 2d in the presence of phosphoryl chloride.

Original languageEnglish
Pages (from-to)87-93
Number of pages7
JournalArkivoc
Volume2003
Issue number5
Publication statusPublished - 2003

Fingerprint

Stereochemistry
Chlorides
Derivatives
Acids
isoquinoline
triethylamine
phosphoryl chloride
phenoxyacetic acid

Keywords

  • β-lactam
  • Isoquinoline
  • Stereochemistry

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Synthesis and stereochemistry of azeto[2,1-a]isoquinolin-2-one derivatives. / Csomós, P.; Martinek, T.; Lázár, L.; Fülöp, F.

In: Arkivoc, Vol. 2003, No. 5, 2003, p. 87-93.

Research output: Contribution to journalArticle

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AU - Lázár, L.

AU - Fülöp, F.

PY - 2003

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