TMSOTf-catalyzed intramolecular seleno-arylation of tethered alkenes was performed using polystyrene-supported succini- midyl selenide as the selenium source. This catalytic process provides an efficient method for th...TMSOTf-catalyzed intramolecular seleno-arylation of tethered alkenes was performed using polystyrene-supported succini- midyl selenide as the selenium source. This catalytic process provides an efficient method for the regioselective synthesis of dihydrocoumarins possessing a seleno-functionality, followed by traceless cleavage of selenium linker to provide dihydrocoumar- ins and coumarins in good yields and purifies.展开更多
基金the National Natural Science Foundation of China(Nos.20802063,21162032)the Foundation of the Key Laboratory of Medicinal Chemistry of Natural Resource(Yunnan University),Ministry of Education,China
文摘TMSOTf-catalyzed intramolecular seleno-arylation of tethered alkenes was performed using polystyrene-supported succini- midyl selenide as the selenium source. This catalytic process provides an efficient method for the regioselective synthesis of dihydrocoumarins possessing a seleno-functionality, followed by traceless cleavage of selenium linker to provide dihydrocoumar- ins and coumarins in good yields and purifies.
