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The Principle of Vinylogy as Applied to Heterocyclic Donor Systems

Chapter
Publication Date:
2012
abstract:
Vinylogy and the reactions inspired by this principle occupy a rewarding position in the arsenal of chemical transformations. This review celebrates this principle, as applied to three enabling carbon-carbon bond formations, the aldol, Mannich, and Michael reactions. Highlighted are those reactions involving heterocyclic vinylogous nucleophilic or pro-nucleophilic candidates, through which myriad of multifunctional molecular frameworks and targets could be synthesized. In this review, we mainly discuss investigations focusing on furan- and pyrrole-based donors, which appeared in the literature during the 2010-2012 triennium.
Iris type:
02.01 Contributo in volume (Capitolo o Saggio)
Keywords:
3.Indirect Mukaiyama-type methodologies; 4.Direct; catalytic methodologies
List of contributors:
Rassu, GLORIA MARIA RITA
Handle:
https://iris.cnr.it/handle/20.500.14243/265121
Book title:
Targets in Heterocyclic Systems - Chemistry and Properties
Published in:
TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES
Journal
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