Issue 0, 1980

A novel reduction of activated olefins by lithium amides

Abstract

Activated olefins of the type Ph2C[double bond, length half m-dash]CXY (X and Y being electronegative substituents) reacted in tetrahydrofuran a low temperature with lithium amides having a hydrogen atom at C-α, to give the corresponding saturated derivatives. The reduction took place by a transfer of a hydride ion from the amide to the activated double bond.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 1267-1269

A novel reduction of activated olefins by lithium amides

U. Melamed and B. Feit, J. Chem. Soc., Perkin Trans. 1, 1980, 1267 DOI: 10.1039/P19800001267

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