An improved method for the synthesis of 2-(p-halobenzyl)-3-aryl-6-methoxybenzofurans as selective ligands for the antiestrogen-binding sites
Ng, S.-C. Kon, O.-L. Sim, K.-Y. Srikanth, N.
Srikanth, N.
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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).
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Synthetic Communications
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Date
1993
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Article