作者:Stefan Bäurle、Sabine Hoppen、Ulrich Koert
DOI:10.1002/(sici)1521-3773(19990503)38:9<1263::aid-anie1263>3.0.co;2-2
日期:1999.5.3
A highly convergent, modular strategy for the total synthesis of the annonaceous acetogenin (-)-mucocin is reported. The remarkable features are the endo-selective formation of the tetrahydropyran ring from an activated epoxide and the stability of the butenolide in the coupling with an organomagnesium compound.
报导了高度聚合的模块化策略,用于合成无
水产
乙酸原(-)-
粘菌素。显着的特征是由活化的
环氧化物选择性地形成
四氢吡喃环,以及
丁烯内酯在与
有机镁化合物偶联时的稳定性。