Diels–Alder cycloadditions of in situ-generated, substituted 2,2-dimethoxycyclohexa-3,5-dienones with olefinic dienophiles resulted in the development of an efficient method for the preparation of highly functionalized bicyclo[2.2.2]oct-5-en-2-ones with good to excellent yields.
原位生成的取代的2,2-二甲氧基环己-3,5-二
壬烯与烯烃二烯亲和物的Diels-Alder环加成反应,导致开发出一种高效方法来制备高度官能化的双环[2.2.2] oct-5-en -2-酮具有良好至优异的产率。