Title of article
Unexpected epimerization and stereochemistry revision of IMDA adducts from sorbate-related 1,3,8-nonatrienes
Author/Authors
Wu، نويسنده , , Jinlong and Yu، نويسنده , , Haihua and Wang، نويسنده , , Yan-yan Xing، نويسنده , , Xinglong and Dai، نويسنده , , Wei-Min، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2007
Pages
5
From page
6543
To page
6547
Abstract
Intramolecular Diels–Alder (IMDA) reaction of two sorbate-related 1,3,8-nonatrienes has been investigated in MeCN at 180 °C for 1.5 h under controlled microwave heating. On checking the crude product mixture before purification, partial epimerization of the major adduct was found during the reaction. After column chromatographic purification over silica gel, only two cis adducts were obtained and their structures have been thoroughly established by X-ray crystallographic analysis. It is concluded that the putative major trans adduct predicted by the IMDA reaction mechanism undergoes facile epimerization at high temperature or in the presence of silica gel. Structural revision on the adducts has been made.
Keywords
intramolecular Diels–Alder reaction , Isomerization , microwave , Stereochemistry , Sorbate , lactone
Journal title
Tetrahedron Letters
Serial Year
2007
Journal title
Tetrahedron Letters
Record number
1856432
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