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AMINO ACIDS AND PEPTIDES: II. SYNTHESIS OF ε-<i>N</i>-METHYL-<scp>L</scp>-LYSINE AND RELATED COMPOUNDS
48
Citations
12
References
1964
Year
Bioorganic ChemistryPeptide EngineeringOrganic ChemistryPeptide SciencePeptide ChemistryChemical BiologyPharmaceutical ChemistryChemical Derivativeα-N-benzoyl-ω-n-p-toluenesulphonylamino AcidBorohydride TreatmentDerivativesBiochemistryε-N-methyl-l-lysine Ethyl EsterPharmacologyEnantioselective SynthesisBiomolecular EngineeringNatural SciencesPeptide LibraryPeptide SynthesisProtein EngineeringMedicineDerivative (Chemistry)Synthetic Chemistry
ε-N-Methyl-L-lysine, ε-N-ethyl-L-lysine, and δ-N-methyl-L-ornithine have been synthesized by alkylation of the α-N-benzoyl-ω-N-p-toluenesulphonylamino acid. ε-N-Methyl-L-lysine was also prepared by the formaldehyde – formic acid methylation of α-N-carbobenzoxy-ε-N-benzyl-L-lysine, obtained by borohydride treatment of α-N-carbobenzoxy-L-lysine in the presence of benzaldehyde. ε-N, ε-N-Dimethyl-L-lysine, ε-N-benzyl-L-lysine, and ε-N-methyl-L-lysine ethyl ester were also prepared.
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