%0 Journal Article %A Raut, Vivek S. %A Jean, Marion %A Vanthuyne, Nicolas %A Roussel, Christian %A Constantieux, Thierry %A Bressy, Cyril %A Bugaut, Xavier %A Bonne, Damien %A Rodriguez, Jean %D 2017 %T Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion Strategy %U https://acs.figshare.com/articles/journal_contribution/Enantioselective_Syntheses_of_Furan_Atropisomers_by_an_Oxidative_Central-to-Axial_Chirality_Conversion_Strategy/4609579 %R 10.1021/jacs.6b11079.s001 %2 https://acs.figshare.com/ndownloader/files/7496215 %K enantiopurities accounting %K Oxidative Central-to-Axial Chirality Conversion Strategy %K enantiomerically %K cp %K chiral furans %K atropoisomeric furans %K oxidation %K conversion percentages %K Enantioselective Syntheses %K Furan Atropisomers %K enantioenriched dihydrofuran precursors %K central-to-axial chirality conversion strategy %X 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. %I ACS Publications