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Le blocage de la lysine par la réaction de M<scp>AILLARD</scp>. I. Synthèse de N‐(désoxy‐1‐<scp>D</scp>‐fructosyl‐1)‐ et N‐(désoxy‐1‐<scp>D</scp>‐lactulosyl‐1)‐<scp>L</scp>‐lysines
82
Citations
17
References
1969
Year
Bioorganic ChemistryEngineeringBiochemistryNatural SciencesLysine DerivativesFormyl DerivativesEt N‐Peptide SynthesisAnalytical ChemistryLe BlocageLiquid ChromatographyChromatographyNatural Product SynthesisEnzymatic ModificationChromatographic AnalysisI. SynthèsePyridine‐formic Acid BuffersBiomolecular Engineering
Abstract The authors describe a specific method for the preparation of Nϵ‐(1‐deoxy‐D‐fructosyl)‐L‐lysine, Nα‐(1‐deoxy‐D‐fructosyl)‐L‐lysine, their formyl derivatives, and Nα‐formyl‐ϵ‐(1‐deoxy‐D‐lactulosyl)‐L‐lysine, as well as Nα, Nϵ‐di‐(1‐deoxy‐D‐fructosyl)‐L‐lysine. After purification by cation‐exchange chromatography using volatile pyridine‐acetic acid or pyridine‐formic acid buffers, these compounds are obtained in the pure state. By thin‐layer chromatography and paper electrophoresis these lysine derivatives can be rapidly separated and identified.
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