New phosphonium ylides by functionalization of triphenylphosphoranylideneacetamide
MJ Wanner, GJ Koomen
Index: Wanner, Martin J.; Koomen, Gerrit-Jan Tetrahedron Letters, 1992 , vol. 33, # 11 p. 1513 - 1516
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Citation Number: 8
Abstract
Abstract Triphenylphosphoranylideneacetamide undergoes Michael reactions with several acceptors, giving rise, apart from the normal Michael adducts, to the formation of different products like glutarimide ylides and stabilized iminophosphoranes. Wittig reactions with these new ylides lead to a variety of α, β-unsaturated carbonyl compounds.
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