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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 15, 1985 - Issue 12
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Original Articles

Generation of 10-Diazolongibornane from Longifolene and Synthesis of Neolongifolene-the Elusive Progenitor of Isolongifolene

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Pages 1107-1111 | Published online: 19 Dec 2006
 

Abstract

Neolongifolene 2, the elusive progenitor of isolongifolene 3, has been synthesised from longifolene in five steps. The strategy consists in generating the crucial longibornyl-10-cation 11 under basic conditions (via 10-diazolongibornane 9 in a protic Bamford-Stevens reaction), which then expels a proton after prior rearrangement, thus affording the target olefin 2; on exposure to any acid, 2 readily collapses into isolongifolene 3.

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