Issue 6, 1983

Novel synthesis of platinum(II) alkenyl compounds via organoboration of platinum(II) acetylides

Abstract

High-yield syntheses of two new types of platinum (II) alkenyl compounds are described: (i) organoboration of trans-[Pt(C[triple bond, length as m-dash]C–H)2(PEt3)2] with R13B (R1= Me, Et, or Pri) leads to (E,E)-trans-[Pt(CH[double bond, length half m-dash]CR1BR12)2-(PEt3)2] and (ii) organoboration of trans-[Pt(C[triple bond, length as m-dash]C–Me)2(PEt3)2] with R13B (R1= Me or Et) leads to (E)-trans-[Pt(C[triple bond, length as m-dash]C–Me)(CMe[double bond, length as m-dash]CR1BR12)(PEt3)2].

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 309-310

Novel synthesis of platinum(II) alkenyl compounds via organoboration of platinum(II) acetylides

A. Sebald and B. Wrackmeyer, J. Chem. Soc., Chem. Commun., 1983, 309 DOI: 10.1039/C39830000309

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