The chirality of the catalyst is essential for achieving enantioselectivity in the N-H insertion reaction. The arrangement of the ligands around the copper center is such that it induces a specific orientation of the reacting species, leading to the preferred formation of one enantiomer of the product.
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FLAMPROP-M-ISOPROPYL
trans-5-phenylsulfanyl-pyrrolidine-1,2-dicarboxylic acid dimethyl ester
(3aR,4R,5R,6aS)-5-(benzoyloxy)hexahydro-4-(iodomethyl)-2H-cyclopentafuran-2-one
Benzofuran, 2-(4-chlorophenyl)-5-nitro-
(3-NONYL-2-OXIRANYL)METHANOL
