Author:
Seebacher Werner,Saf Robert,Brun Reto,Kaiser Marcel,Weis Robert
Abstract
Under strongly basic conditions (6SR,7SR)-4-amino-6,7-diphenylbicyclo[2.2.2]octan-2-ones isomerized regioselectively in position 6 giving their (6RS,7SR) analogues. The structure of the new products was established with the aid of NMR experiments.Key words: aminobicyclo[2.2.2]octanones, isomerization, structure elucidation.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
4 articles.
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