Issue 8, 1997

Synthesis of conjugated dienes from vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans via zirconocene-mediated deoxygenation

Abstract

The zirconocene-mediated reaction of vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans proceeds via deoxygenation, yielding conjugated dienes.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 1095-1098

Synthesis of conjugated dienes from vinyl epoxides, vinyl acetonides and 2,5-dihydrofurans via zirconocene-mediated deoxygenation

S. Kim and K. Hee Kim, J. Chem. Soc., Perkin Trans. 1, 1997, 1095 DOI: 10.1039/A608593H

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