An efficient and novel methodology to access phenolic glycosides has been established by using coppermediated coupling reaction of aryl boronic acids with hemiacetals.The reaction takes place normally in the presence ...An efficient and novel methodology to access phenolic glycosides has been established by using coppermediated coupling reaction of aryl boronic acids with hemiacetals.The reaction takes place normally in the presence of Cu(OAc)_2(1.0 equiv.)and pyridine(2.0 equiv.)at 40℃.This protocol distinguishes itself by wide substrate scope,operational simplicity and giving rise to a myriad of phenolic glycosides in good to excellent yields.展开更多
基金financially supported by the National Key R&D Program of China (No. 2018YFA0507602)the National Natural Science Foundation of China (Nos. 21572012, 21772006)the State Key Laboratory of Drug Research (No. SIMM1803KF-02)
文摘An efficient and novel methodology to access phenolic glycosides has been established by using coppermediated coupling reaction of aryl boronic acids with hemiacetals.The reaction takes place normally in the presence of Cu(OAc)_2(1.0 equiv.)and pyridine(2.0 equiv.)at 40℃.This protocol distinguishes itself by wide substrate scope,operational simplicity and giving rise to a myriad of phenolic glycosides in good to excellent yields.
基金supported by the National Natural Science Foundation of China(No.20472068)Specialized Research Fund for the Doctoral Program of Higher Education(No.200807360001)Key Laboratory of Eco-Environment -Related Polymer Materials of Ministry of Education(Northwest Normal University)
文摘2,5-Disubstituted tetrahydrofurans were obtained from lactones and organozinc halides in moderate to high yield in the presence of Lewis acids.
