Issue 16, 1989

Enantioselective telomerization of butadiene with formaldehyde yielding divinyltetrahydropyrans

Abstract

The enantioselective telomerization of butadiene with formaldehyde, catalysed by Pd(OAc)2 plus bidentate phosphine ligands, yielding 2,5-divinyltetrahydropyran in optical purity up to 36% is described; a fused-silica capillary with a chiral stationary phase of cyclodextrin has been prepared and successfully applied in product analysis for the first time.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1151-1152

Enantioselective telomerization of butadiene with formaldehyde yielding divinyltetrahydropyrans

W. Keim, W. Meltzow, A. Koehnes and T. Roethel, J. Chem. Soc., Chem. Commun., 1989, 1151 DOI: 10.1039/C39890001151

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