Enantioselective Syntheses of Furan Atropisomers by an Oxidative Central-to-Axial Chirality Conversion Strategy

J Am Chem Soc. 2017 Feb 15;139(6):2140-2143. doi: 10.1021/jacs.6b11079. Epub 2017 Feb 2.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't