Phosphane-catalyzed Knoevenagel condensation: a facile synthesis of α-cyanoacrylates and α-cyanoacrylonitriles

Yadav, Jhillu S. ; Subba Reddy, Basi V. ; Basak, Ashok K. ; Visali, Boddapati ; Venkat Narsaiah, Akkirala ; Nagaiah, Kommu (2004) Phosphane-catalyzed Knoevenagel condensation: a facile synthesis of α-cyanoacrylates and α-cyanoacrylonitriles European Journal of Organic Chemistry, 2004 (3). pp. 546-551. ISSN 1434-193X

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.20...

Related URL: http://dx.doi.org/10.1002/ejoc.200300513

Abstract

Triphenylphosphane (TPP) has been utilized as a novel and efficient catalyst for the Knoevenagel condensation of aldehydes with acidic methylene compounds such as ethyl cyanoacetate and malononitrile to afford substituted olefins. The reaction proceeds smoothly under mild and solvent-free conditions and the products are obtained in excellent yields with an E-geometry. This method is applicable for a wide range of aldehydes including aromatic, aliphatic and heterocyclic substrates. Microwave irradiation has been used to achieve enhanced reaction rates and improved yields.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Aldehydes; Knoevenagel Reaction; Microwave Activation; Phosphanes
ID Code:62746
Deposited On:24 Sep 2011 04:49
Last Modified:24 Sep 2011 04:49

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