10.1021/jacs.6b11079.s001 Vivek S. Raut Vivek S. Raut Marion Jean Marion Jean Nicolas Vanthuyne Nicolas Vanthuyne Christian Roussel Christian Roussel Thierry Constantieux Thierry Constantieux Cyril Bressy Cyril Bressy Xavier Bugaut Xavier Bugaut Damien Bonne Damien Bonne Jean Rodriguez Jean Rodriguez Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion Strategy American Chemical Society 2017 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 00:00:00 Journal contribution https://acs.figshare.com/articles/journal_contribution/Enantioselective_Syntheses_of_Furan_Atropisomers_by_an_Oxidative_Central-to-Axial_Chirality_Conversion_Strategy/4609579 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.