ETUDE DE NOUVELLES REACTIONS RADICALAIRES ET APPLICATION A LA SYNTHESE D'ALCALOIDES

ORSAY-PARIS 11-BU Sciences (914712101) / SudocSudocFranceF

Enantioselective Synthesis of 3,3-Difluoropyrrolidin-4-ol, a Valuable Building Block in Medicinal Chemistry

In this paper, we report for the first time two enantioselective routes to 4,4-difluoropyrrolidin-3-ol, a valuable building block in medicinal chemistry. In the first route, we took advantage of the <i>C</i>₂ symmetry of (3<i>R</i>,4<i>R</i>)-3,4-dihydroxypyrrolidine in which the desired chirality was derived from the chiral pool (l-(+)-tartaric acid). In the second route, we efficiently assembled the pyrrolidine ring in the presence of a <i>gem</i>-difluoro moiety to avoid using potentially hazardous deoxofluorinating reagents and subsequently introduced the chirality by a stereoselective iridium–diamine-catalyzed asymmetric transfer hydrogenation reaction