Saturated heterocycles. 176 Synthesis and steric structure of quaternary azeto[2,1‐a]isoquinoline stereoisomers

G. Bernáth, Ferenc Fölöp, Judit Árva, Jenö Kóbor, P. Sohár

Research output: Article

7 Citations (Scopus)

Abstract

Starting from 1‐substituted azeto[2,1‐a]isoquinoline diastereomers, a number of quaternary salts were prepared. The reactions leading to the quaternary salts were stereospecific, independently of the configuration at C‐1, resulting in diastereomers. The steric structures of the new compounds were proved by nmr spectroscopy.

Original languageEnglish
Pages (from-to)353-357
Number of pages5
JournalJournal of Heterocyclic Chemistry
Volume28
Issue number2
DOIs
Publication statusPublished - 1991

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Stereoisomerism
Salts
Spectroscopy
isoquinoline

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

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abstract = "Starting from 1‐substituted azeto[2,1‐a]isoquinoline diastereomers, a number of quaternary salts were prepared. The reactions leading to the quaternary salts were stereospecific, independently of the configuration at C‐1, resulting in diastereomers. The steric structures of the new compounds were proved by nmr spectroscopy.",
author = "G. Bern{\'a}th and Ferenc F{\"o}l{\"o}p and Judit {\'A}rva and Jen{\"o} K{\'o}bor and P. Soh{\'a}r",
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AU - Bernáth, G.

AU - Fölöp, Ferenc

AU - Árva, Judit

AU - Kóbor, Jenö

AU - Sohár, P.

PY - 1991

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