Issue 13, 1996

Palladium-catalysed carbonyl allylation by 2-methylenepropane-1,3-diol

Abstract

2-Methylenepropane-1,3-diol first allylates an aldehyde exclusively at the allylic alcohol moiety at room temperature and then, at 50 °C, allylates another aldehyde also at the allylic alcohol moiety, in the presence of a catalytic amount of PdCl2(PhCN)2 with tin(II) chloride.

Article information

Article type
Paper

Chem. Commun., 1996, 1585-1586

Palladium-catalysed carbonyl allylation by 2-methylenepropane-1,3-diol

Y. Masuyama, M. Kagawa and Y. Kurusu, Chem. Commun., 1996, 1585 DOI: 10.1039/CC9960001585

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