The Journal of Organic Chemistry · 2012 · 22 citations · 38 references
Medicinal ChemistryAntimicrobial Drug DiscoveryDerivativesUreidomuraymycidine DerivativesBiochemistryNatural SciencesMedicineOrganic ChemistryOligopeptide MoietyStereoselective SynthesisChemical BiologyPharmacologyLactone 4APharmaceutical ChemistrySynthetic ChemistryDrug DiscoveryNatural Product Synthesis
One of the key constituents of the muraymycins is the 6-membered cyclic guanidine, (2S,3S)-muraymycidine (or epi-capreomycidine). In order to diversify the structure of the oligopeptide moiety of the muraymycins for thorough structure-activity relationship studies, we have developed a highly stereoselective synthesis of ureidomuraymycidine derivatives with the lactone 4a.
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Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids
Stephan J. Zuend, Matthew P. Coughlin, Mathieu P. Lalonde et al. · Nature · 2009 · 384 citations · Full text