An Improved Method for the Synthesis of 2-(p-Halobenzyl)-3-aryl-6-methoxybenzofurans as Selective Ligands for the Antiestrogen-Binding Sites
摘要:
A series of 2-(p-fluorobenzyl)-3-aryl-6-methoxybenzofurans has been prepared in good yields in a two-step sequence from the corresponding benzylidencoumaranones (aurones).