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Enantioselective Synthesis of Biphenols from 1,4-Diketones by Traceless Central-to-Axial Chirality Exchange

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NIAID Data Ecosystem2026-03-06 收录
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A method for the enantioselective synthesis of biphenols from readily prepared 1,4-diketones is reported. Key to the success of this method is the highly selective transfer of central to axial chirality during a double aromatization event triggered by BF3·OEt2. On the basis of X-ray crystallographic data, a stereochemical model for this chirality exchange process is put forth.

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2011-01-12
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