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ChemInform Abstract: Efficient, Direct α-Methylenation of Carbonyls Mediated by Diisopropylammonium Trifluoroacetate
Journal article   Peer reviewed

ChemInform Abstract: Efficient, Direct α-Methylenation of Carbonyls Mediated by Diisopropylammonium Trifluoroacetate

Alejandro Bugarin, Kyle D Jones and Brian T Connell
Chemical communications : Chemcomm / the Royal Society of Chemistry, Vol.41(28), pp.no-no
07-13-2010

Abstract

aldehydes (benzene compounds) benzopyran derivatives cyclopentane derivatives hydrogenated naphthalene derivatives ketones (benzene compounds) olefination rings with 7 or more members
Excerpt: Molecules containing the α,β-unsaturated carbonyl functionality are commonly utilized as substrates for a range of chemical transformations, including nucleophilic addition,1 Michael addition,2 the Morita–Baylis–Hillman reaction,3 Diels–Alder reaction,4 and several organo-catalytic reactions.5 The importance of the α-methylene moiety is amplified by its presence in numerous biologically active natural products.6 α-Methylenation has attracted attention because it is generally an atom economical method for conversion of simple carbonyl compounds to their α,β-unsaturated derivatives.
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