Azide-Free Synthesis of <i>N</i>-Alkyliminophosphoranes from Phosphines and Hydroxylamine Derivatives
Eric Falk, Allegra Franchino, Teresa Horak, Laura Gürtler, Bill Morandi
Abstract
-alkyliminophosphoranes from phosphines that does not use potentially hazardous alkyl azides is reported. Under iron catalysis, a hydroxylamine-derived triflic acid salt oxidizes phosphines to a wide range of iminophosphorane triflic acid salts. Diphosphines afford phosphine-iminophosphoranes that can serve as ligands in transition metal complexes. The developed method can be employed in the synthesis of mixed diiminophosphoranes and in a traceless Staudinger ligation.
Topics & Concepts
ChemistryTriflic acidDiphosphinesPhosphineHydroxylamineAzideOrganic chemistryCombinatorial chemistryAlkylStaudinger reactionSalt (chemistry)CatalysisMedicinal chemistryClick Chemistry and ApplicationsChemical Synthesis and AnalysisSynthesis and Catalytic Reactions