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A rapid and efficient CsF catalyzed tandem Knoevenagel-Michael reaction
Journal article   Peer reviewed

A rapid and efficient CsF catalyzed tandem Knoevenagel-Michael reaction

Khalid Mohammed Khan, Imran Khan, Shahnaz Perveen and Muhammad Imran Malik
Journal of fluorine chemistry, Vol.158, pp.1-5
01/02/2014

Abstract

Chemistry Chemistry, Inorganic & Nuclear Chemistry, Organic Physical Sciences Science & Technology
A simple, experimentally rapid and efficient CsF catalyzed tandem Knoevenagel-Michael reaction protocol is developed for the synthesis of a series of functionalized 9-(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-enyl)-3,3-dimethyl-2,3,4,9-tetrahydro-1H-xanthen-1-one (1-7) by reacting dimedone with substituted salicylaldehydes. The use of CsF as a catalyst allowed reactions under moderate conditions and resulted in better yields. (C) 2013 Elsevier B.V. All rights reserved.

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