Une synthèse hautement stéréosélective de diènes conjugués (E)

R Bloch, J Abecassis, D Hassan

Index: Bloch, R.; Abecassis, J.; Hassan, D. Canadian Journal of Chemistry, 1984 , vol. 62, p. 2019 - 2024

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Citation Number: 23

Abstract

A general method for the preparation of (E) terminal conjugated dienes was developed by the flash thermolysis of 2-substituted 2, 5-dihydrothiophene-1, 1-dioxides generated by a retro Diels-Alder reaction. This process allows the obtention of conjugated dienes, bearing or not a functionality (alcohols, esters), with an excellent stereoisomeric purity (in general higher than 98%). An application to the synthesis of (E)-9, 11-dodecadien-1-yl acetate, the ...