Ruthenium-Catalyzed C–H Hydroxylation in Aqueous Acid Enables Selective Functionalization of Amine Derivatives
Author:
Affiliation:
1. Department of Chemistry, Stanford University, 337 Campus Drive, Stanford, California 94305, United States
2. Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112, United States
Funder
Center for Selective C-H Functionalization, National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.7b05469
Reference32 articles.
1. Alkane C–H Oxygenation Catalyzed by Transition Metal Complexes
2. Evolution of C–H Bond Functionalization from Methane to Methodology
3. The medicinal chemist's toolbox for late stage functionalization of drug-like molecules
4. Accessing Drug Metabolites via Transition-Metal Catalyzed C−H Oxidation: The Liver as Synthetic Inspiration
5. Stereospecific Alkane Hydroxylation with H2O2 Catalyzed by an Iron(II)−Tris(2-pyridylmethyl)amine Complex
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