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.
The Principle of Vinylogy as Applied to Heterocyclic Donor Systems
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.File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


