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Regio et stereochimie de la reduction de derives d'alcools propargyliques catalysee par un complexe de palladium (O)
Authors:Yann Colas  Bernard Cazes  Jacques Gore
Institution:Laboratoire de Chimie Organique 1, ERA 611 du CNRS, Université Claude Bernard Lyon I, E.S.C.I.L., 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cédex, France.
Abstract:Regio and stereoselectivity of the palladium catalyzed reduction of propargylic halides and esters is greatly influenced by the nature of the hydride donor as by the leaving group. Best results in allene formation are observed in the reduction by lithium triethyl-borohydride of mesylates and phosphates. In the former case, reaction occurs with anti displacement of the sulfonyl group.
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