Title of article
On the Diels–Alder reactions and the Lewis acid induced rearrangements of 6-fumaryl 1,3,8-nonatrienes
Author/Authors
Clarke، نويسنده , , Paul A. and Davie، نويسنده , , Rebecca L. and Peace، نويسنده , , Simon، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
2753
To page
2756
Abstract
6-Fumaryl 1,3,8-nonatrienes substituted at the C5 position by a vinyl group were found to undergo competing tandem sigmatropic rearrangement/Diels–Alder cyclisation when heated under standard Diels–Alder cyclisation conditions. This rearrangement became the exclusive pathway when the reactions were performed in the presence of a Lewis acid.
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1651024
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