Affiliation:
1. Institut für Pharmazie der Freien Universität Berlin
Abstract
The mercuric EDTA dehydrogenation of the isomeric 1,2- and 2,1-(phenyl-pyrrolidino)-ethanols yields with two electron removal the corresponding oxazolidines. The analogous 1,2- and 2,1-(amino-phenyl)pyrrolidines by double dehydrogenation produce the amidines resp. by subsequent hydrolysis the lactams. An explanation for the different course of the reaction is given
Cited by
12 articles.
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