6533b874fe1ef96bd12d6373

RESEARCH PRODUCT

Diastereoselective Synthesis of Enantioenriched Trifluoromethylated Ethylenediamines and Isoindolines Containing Two Stereogenic Carbon Centers by Nucleophilic Trifluoromethylation Using HFC-23.

Takuya SaitoSantos FusteroDaniel M. SedgwickYamato FujihiraNorio ShibataNorio ShibataKazuki Hirano

subject

chemistry.chemical_compoundNucleophilic additionNucleophilechemistryFluoroformTrifluoromethylationOrganic ChemistryEthylenediamineschemistry.chemical_elementCarbonCombinatorial chemistryStereocenter

description

Fluoroform, HFC-23, is an industrial byproduct from the synthesis of polytetrafluoroethylene and is a vastly underused resource; however, its physicochemical properties have hindered progress toward synthetic uses. Herein, we describe the use of HFC-23 as a cheap trifluoromethylating agent in two reactions for the highly diastereoselective synthesis of medicinally attractive chiral amines with two stereogenic carbon centers: a base-dependent, stereodivergent nucleophilic addition to synthesize enantioenriched vicinal diamines and a tandem nucleophilic addition/aza-Michael sequence toward enantioenriched isoindolines.

10.1021/acs.joc.0c00796https://pubmed.ncbi.nlm.nih.gov/32421330