Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion Strategy Vivek S. Raut Marion Jean Nicolas Vanthuyne Christian Roussel Thierry Constantieux Cyril Bressy Xavier Bugaut Damien Bonne Jean Rodriguez 10.1021/jacs.6b11079.s001 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. 2017-01-20 00:00:00 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