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 Hiranosubject
chemistry.chemical_compoundNucleophilic additionNucleophilechemistryFluoroformTrifluoromethylationOrganic ChemistryEthylenediamineschemistry.chemical_elementCarbonCombinatorial chemistryStereocenterdescription
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.
year | journal | country | edition | language |
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2020-05-18 | The Journal of organic chemistry |