Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1, 3, 5-triols featuring supramolecular recognition properties. Issue 6 (9th January 2020)

• Record Type: Journal Article
• Authors: Sperandio, Céline; Rodriguez, Jean; Quintard, Adrien
• Is Part Of: Chemical science. Volume 11:Issue 6(2020)
• Page Start: 1629
• Page End: 1635
• Publication Date: 2020-01-09
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9sc05196a
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : An enantioselective aldolization on perfluorinated aldehydes has been developed. The reaction can create in one step ketodiols, precursors of crucial perfluorinated 1, 3, 5-triols featuring selective chiral anion recognition ability. Abstract : Fluorine is able to confer unique properties to organic molecules but the scarcity of natural organofluorine sources renders the development of new synthetic methods highly desirable. Using a chiral BOX/Cu combination, enantioselective decarboxylative aldolization of perfluorinated aldehydes has been developed. Most notably, the reaction occurring under mild conditions and with high enantiocontrol can create ketodiols in one single synthetic operation, which are precursors of crucial perfluorinated 1, 3, 5-triols. In addition, the reaction performed with chloral, validates the proposed transition state model based on steric interactions and provides the first enantioselective synthesis of hexachlorinated ketodiol of great synthetic utility. The ability of perfluorinated 1, 3, 5-triols to form a central hydrogen-bonding framework allows strong coordination of anions and the chirality obtained through the catalyst-controlled synthetic sequence demonstrates the selective chiral anion recognition ability of polyols.