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 / Zanardi, Franca; G., Rassu; Battistini, Lucia; Curti, Claudio; Sartori, Andrea; Casiraghi, Giovanni. - In: TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES. - ISSN 1724-9449. - STAMPA. - 16:(2012), pp. 56-89.

The Principle of Vinylogy as Applied to Heterocyclic Donor Systems

ZANARDI, Franca;BATTISTINI, Lucia;CURTI, Claudio;SARTORI, Andrea;CASIRAGHI, Giovanni
2012-01-01

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.
2012
9788886208727
The Principle of Vinylogy as Applied to Heterocyclic Donor Systems / Zanardi, Franca; G., Rassu; Battistini, Lucia; Curti, Claudio; Sartori, Andrea; Casiraghi, Giovanni. - In: TARGETS IN HETEROCYCLIC SYSTEMS: CHEMISTRY AND PROPERTIES. - ISSN 1724-9449. - STAMPA. - 16:(2012), pp. 56-89.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2621246
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