4.7 Article

Aza-Baylis-Hillman reactions of N-(arylmethylene) diphenylphosphinamidies with activated olefins in the presence of various Lewis bases

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 346, Issue 9-10, Pages 1205-1219

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200404081

Keywords

N-(arylmethylene)diphenylphosphin-amide; aza-Baylis-Hillman reactions; DABCO, Lewis bases; organic catalysis; phosphanes

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The aza-Baylis-Hillman reactions of N-(arylmethylene)diphenylphosphinamides with methyl vinyl ketone (MVK), methyl acrylate, acrylonitrile, ethyl vinyl ketone (EVK), phenyl vinyl ketone (PVK), phenyl acrylate, 2-cyclopenten-1-one, 2-cyclohexen-1-one have been systemically investigated in the presence of various Lewis bases. The Lewis base and solvent effects in these reactions have been discussed. A new class of double aza-Baylis-Hillman reactions (in some cases exclusively) and their further transformations including catalytic, asymmetric version in the presence of chiral nitrogen and phosphine Lewis bases have been disclosed in this paper.

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