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2‐Amino‐2‐oxazolines, III: Synthesis, Structure, and Preliminary Pharmacological Evaluation of Cycloaddition Compounds with Unsaturated Carboxylic Esters
Author(s) -
Forfar Isabelle,
Jarry Christian,
Leger JeanMichel,
Carpy Alain
Publication year - 1990
Publication title -
archiv der pharmazie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 61
eISSN - 1521-4184
pISSN - 0365-6233
DOI - 10.1002/ardp.19903231105
Subject(s) - chemistry , cycloaddition , stereochemistry , carboxylic acid , organic chemistry , catalysis
The reaction of 5‐substituted 2‐amino‐2‐oxazolines with unsaturated carboxylic esters yielded 2,3,5,6‐tetrahydro‐ and 2,3‐dihydro‐7 H ‐oxazolo[3,2‐ a ]pyrimidin‐7‐ones. The structure of these compounds was established by IR‐ and NMR‐spectra and by X‐ray crystallography. They were tested for anti‐arrhythmic and hypocholesterolemic activities.

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