Publication | Closed Access
Synthesis of Biologically Relevant Compounds by Ruthenium Porphyrin Catalyzed Amination of Benzylic C–H Bonds
29
Citations
53
References
2014
Year
Benzylic C–h BondsEngineeringBiochemistryBiologically Relevant CompoundsNatural SciencesDiversity-oriented SynthesisCatalytic MethodologyOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistryRuthenium Porphyrin ComplexesSynthetic ChemistryBiomolecular EngineeringMethyl L-3-phenyllactate
Herein we report the catalytic activity of ruthenium porphyrin complexes to promote the amination of benzylic C–H bonds by aryl azides, yielding α- and β-amino esters. The catalytic methodology is also effective to synthesize two derivatives of methyl l-3-phenyllactate in order to convert one of them into the corresponding β-lactam. The catalytic experimental conditions have been optimized on the basis of a preliminary mechanistic investigation which underlines the pivotal role of the substrate concentration to maximize the reaction productivity.
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