Abstract
A catalytic, two-step protocol for the expedient synthesis of anti-2,4-disubstituted tetrahydrofurans is described. In the first step, an enantioselective and regioselective Pd-catalyzed Hayashi-Heck arylation was developed using (R)-hexaMeOBiphep to generate 5-aryl-2,3-dihydrofurans. A subsequent Rh-catalyzed hydroformylation step proceeds at low Rh loading with high regio- and diastereoselectivity for the anti-2,4-disubstituted tetrahydrofuran isomer. Key to the development of the hydroformylation reaction was the utilization of either (R)-Me-i-Pr-INDOLphos or (R,R)-Ph-BPE to control the regioselectivity and provide the kinetic product isomer.
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