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|Title:||An improved method for the synthesis of 2-(p-halobenzyl)-3-aryl-6-methoxybenzofurans as selective ligands for the antiestrogen-binding sites||Authors:||Ng, S.-C.
|Issue Date:||1993||Citation:||Ng, S.-C.,Kon, O.-L.,Sim, K.-Y.,Srikanth, N. (1993). An improved method for the synthesis of 2-(p-halobenzyl)-3-aryl-6-methoxybenzofurans as selective ligands for the antiestrogen-binding sites. Synthetic Communications 23 (13) : 1843-1853. ScholarBank@NUS Repository.||Abstract:||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).||Source Title:||Synthetic Communications||URI:||http://scholarbank.nus.edu.sg/handle/10635/52781||ISSN:||00397911|
|Appears in Collections:||Staff Publications|
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