Publication | Closed Access
A Biomimetic Approach to Lanthionines
23
Citations
57
References
2011
Year
Bioorganic ChemistryEngineeringBiomimetic ApproachOrganic ChemistryAsymmetric Sulfa-michael AdditionsChemistryBiomimetic ChemistryMedicinal ChemistryStereoselective SynthesisDerivativesBiochemistryDiversity-oriented SynthesisNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringD-cysteine DerivativesNatural SciencesUnusual Bis-α-amino AcidsDerivative (Chemistry)Synthetic Chemistry
The asymmetric sulfa-Michael additions of appropriately protected L- and D-cysteine derivatives to new chiral dehydroamino acid derivatives have been developed as key steps in the synthesis of biologically important cysteine derivatives, such as lanthionine (Lan) and β-methyllanthionine (MeLan), which are unusual bis-α-amino acids found in the emerging lantibiotics such as nisin.
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