Raut, Vivek S. Jean, Marion Vanthuyne, Nicolas Roussel, Christian Constantieux, Thierry Bressy, Cyril Bugaut, Xavier Bonne, Damien Rodriguez, Jean Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion Strategy For the first time, enantiomerically enriched atropoisomeric furans have been accessed using a central-to-axial chirality conversion strategy. Hence, oxidation of the enantioenriched dihydrofuran precursors gave rise to axially chiral furans with high enantiopurities accounting from excellent conversion percentages (cp) in most cases. enantiopurities accounting;Oxidative Central-to-Axial Chirality Conversion Strategy;enantiomerically;cp;chiral furans;atropoisomeric furans;oxidation;conversion percentages;Enantioselective Syntheses;Furan Atropisomers;enantioenriched dihydrofuran precursors;central-to-axial chirality conversion strategy 2017-01-20
    https://acs.figshare.com/articles/journal_contribution/Enantioselective_Syntheses_of_Furan_Atropisomers_by_an_Oxidative_Central-to-Axial_Chirality_Conversion_Strategy/4609579
10.1021/jacs.6b11079.s001