FACILE AND METAL-FREE SYNTHESIS OF ISOFLAVONES USING α-ARYL-β,β-DITOSYLOXY KETONES

Considering the drawbacks associated with available synthetic methodologies of isoflavones, herein we have reported a metal-free and eco-friendly approach to these natural products. In the present study, we have carried out the synthesis of eight isoflavone derivatives 7a-7h using α-aryl-β,β-ditosyloxy ketones protocol. Initially, we have protected the 2’-hydroxy group of respective chalcone moiety in order to remove its interference under reaction conditions. The 2’-protected chalcones were then subjected to 1,2-aryl migration by being treated with hydroxy(tosyloxy)iodobenzene (HTIB) reagent in a non-nucleophilic solvent (CH2Cl2). This migration furnished the formation of α-aryl-β,β-ditosyloxy ketones via C-C bond formation from their corresponding chalcones in moderate to good yields (55-82%). The ambiguity regarding the exact molecular structure of the α-aryl-β,β-ditosyloxy ketones was examined through the single crystal X-ray diffraction data. At last, the synthesis of isoflavones was carried in moderate to good yields (50-80%) out by performing the reaction of α-aryl-β,β-ditosyloxy ketones with sodium hydroxide in aqueous methanol.