Issue 6, 1997

Synthesis of 3-(p-Halobenzyl)-4-aryl-2H-chromenes as Selective Ligands for Antiestrogen-binding Sites

Abstract

A series of 3-(p-halobenzyl)-4-aryl-2H-chromenes is prepared in good yields via a two-step sequence from the corresponding 3-benzylidenechromanones (homoisoflavanones).

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 202-203

Synthesis of 3-(p-Halobenzyl)-4-aryl-2H-chromenes as Selective Ligands for Antiestrogen-binding Sites

N. Srikanth, S. Ng, K. Sim and O. Kon, J. Chem. Res. (S), 1997, 202 DOI: 10.1039/A700565B

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