摘要
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.
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.
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