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BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Synthesis of New Polysubstituted Pyrrolidinones with Potential Biological Activity

  • Nikola T. Burdzhiev and Elena R. Stanoeva EMAIL logo

The reaction of succinic anhydride and N-benzylidene-benzylamine gave rise to the corresponding substituted trans-5-oxopyrrolidine-3-carboxylic acid, which was transformed stereoselectively into two series of compounds. The first one consists of carboxamides, and the second one includes aminomethyl derivatives. The compounds prepared incorporate both a pyrrolidinone part and other nitrogen containing heterocyclic fragments of pharmacological interest.

Received: 2007-10-31
Published Online: 2014-6-2
Published in Print: 2008-3-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

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