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3-Pyrrolidinones: Michael Addition and Schmidt Rearrangement Reactions
Journal article   Peer reviewed

3-Pyrrolidinones: Michael Addition and Schmidt Rearrangement Reactions

F. A. Amer, M. Hammouda, A. A. S. El-Ahl and B. F. Abdel-Wahab
Synthetic communications, Vol.39(3), pp.416-425
13/01/2009

Abstract

3-pyrrolidinones Arylidenemalononitriles isatin-3-ylidines Michael addition Schmidt rearrangement
Various spiro-pyrano[3,2-b]pyrrolo-2-oxoindolines 3a-d and dicyano-pyrano[3,2-b]pyrroles 5a-e have been synthesized in the present study by Michael addition of 3-pyrrolidinones 1 to isatin-3-ylidenes 2 and arylidenemalononitrile 4. Hexahydro-4-oxo-1-aryl-pyrimidine-5-carboxylic acids 7a,b were synthesized from 1 by Schmidt rearrangement.

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