A completely stereoselective intramolecular diels-alder reaction in the substituted cyclohexanol series
作者:A. Alexakis、D. Jachiet、L. Toupet
DOI:10.1016/s0040-4020(01)85131-0
日期:1989.1
Subtituted dienyl cyclohexanols, obtained through opening of cyclohexene oxide by dienyl aluminum reagents, are easily esterified with acryloyl, crotonyl or methacryoyl chloride or with maleic anhydride. These esters undergo a completely stereoselective Lewis acid catalyzed Diesels-Alder reaction. The obtained product were characterized by X-ray crystallography.