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Pallado-catalysed P-arylations and P-vinylation of 2-hydrogeno-2-oxo-1,4,2-oxazaphosphinanes
Journal article   Peer reviewed

Pallado-catalysed P-arylations and P-vinylation of 2-hydrogeno-2-oxo-1,4,2-oxazaphosphinanes

Jean-Luc Pirat, Jérôme Monbrun, David Virieux and Henri-Jean Cristau
Tetrahedron, Vol.61(29), pp.7029-7036
02/05/2005

Abstract

Arylphosphinate Aminoalkylarylphosphinic acid Vinylation Arylation Pallado-catalyse
A simple and effective preparation of 2-aryl- (or 2-vinyl)-1,4,2-oxazaphosphinanes, phosphorus analogues of aryl-morpholinols has been developed, involving palladium catalysed coupling of aryl (or vinyl)-halides with 2-H-1,4,2-oxazaphosphinane in presence of triethylamine. A deprotection step was also proposed to afford the corresponding P-aryl-α-aminobenzylphosphinic acid
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