2026-06-26T15:45:42Zhttps://docta.ucm.es/rest/oai/request

oai:docta.ucm.es:20.500.14352/993842024-07-02T23:46:39Zcom_20.500.14352_14col_20.500.14352_15

Donohoe, Timothy Callens, Cedric Flores Aguilar-Amat, Aída Mesch, Stefanie Poole, Darren Roslan, Ishmael 2024-02-06T11:21:34Z 2024-02-06T11:21:34Z 2011 1433-7851 10.1002/anie.201103293 https://hdl.handle.net/20.500.14352/99384 1521-3773 https://doi.org/10.1002/anie.201103293 https://www.wiley-vch.de/en/shop/journals/276 A viable nitrogen source for the aminohydroxylation reaction of terminal alkenes: By adding a N-O based reoxidant onto an amino acid acyl carbon atom, compounds were obtained that facilitated catalytic turnover and also promoted the conjugation of an amino acid with an alkene. High levels of regioselectivity were observed, as well as good stereoselectivity induced by catalytic amounts of a chiral ligand. eng restricted access Amino Acid-Based reoxidants for aminohydroxylation: Application to the Construction of Amino Acid–Amino Alcohol Conjugates journal article