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  • Chiral thiophosphoramide and selenophosphoramide ligands in the Cu(I)-promoted catalytic enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and pyrrole-2,5-dione derivatives
  • Add time:07/26/2019         Source:sciencedirect.com

    Chiral C2-symmetric diphenylthiophosphoramide ligand L1 prepared from C2-symmetric (1S,2S)-(−)-1,2-diphenylethylenediamine was found to be a fairly effective chiral ligand for Cu(I)-promoted 1,3-dipolar cycloaddition of imines and pyrrole-2,5-dione derivatives to give the corresponding adducts in moderate enantioselectivities and good yields.

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