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