Enantioselective intramolecular C–H amination of aliphatic azides by dual ruthenium and phosphine catalysis

Chemistry 01 natural sciences 0104 chemical sciences
DOI: 10.1039/c9sc00054b Publication Date: 2019-01-29T07:04:52Z
ABSTRACT
By combining a chiral-at-metal ruthenium catalyst with catalytic amounts of tris(p-fluorophenyl)phosphine (both 1 mol%), the challenging catalytic enantioselective ring-closing C(sp3)-H amination of unactivated aliphatic azides has been achieved with high enantioselectivities.
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