Issue 10, 1981

Facile P–C bond cleavage in the reactions of nitrile oxides with zerovalent triphenylphosphine platinum complexes

Abstract

Stable nitrile oxides react with Pt(PPh3)2L (L = PPh3,C2H4) to give 1 : 1 products; X-ray studies show that the nitrile oxide is deoxygenated by triphenyl-phosphine and that a phenyl group migrates to the platinum atom to give the complexes [Pt(Ph)(OPPh2)(RCN)(PPh3)].

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 446-448

Facile P–C bond cleavage in the reactions of nitrile oxides with zerovalent triphenylphosphine platinum complexes

W. Beck, M. Keubler, E. Leidl, U. Nagel, M. Schaal, S. Cenini, P. Del Buttero, E. Licandro, S. Maiorana and A. C. Villa, J. Chem. Soc., Chem. Commun., 1981, 446 DOI: 10.1039/C39810000446

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