Insights into base-free OsO4-catalyzed aminohydroxylations employing chiral ligands.

Insights into base-free OsO4-catalyzed aminohydroxylations employing chiral ligands.
Tetrahedron. 2019 Feb 22;75(8):945-948
Authors: Cardon JM, Coombs JC, Ess DH, Castle SL
Abstract
Attempts to perform the OsO4-catalyzed enantioselective base-free aminohydroxylation of β,β-disubstituted enoates are described. Low yields and racemic products were obtained in the presence of standard chiral ligands, suggesting the occurrence of a "Second Cycle" process due to slow hydrolysis of the amino alcohol product from the Os metal center. Support for this hypothesis was provided by the slightly improved enantioselectivity (60:40 er) obtained with an amino alcohol ligand. Based on density functional theory calculations, it is proposed that the lack of significant enantioselectivity is due to a low-energy (3 + 2) oxo/imido cycloaddition transition state without the chiral ligand in the Second Cycle that outcompetes protonolysis in the First Cycle.
PMID: 30774161 [PubMed]

Source: Tetrahedron - February 19, 2019 Category: Chemistry Authors: Cardon JM, Coombs JC, Ess DH, Castle SL Tags: Tetrahedron Source Type: research