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.