Publication | Open Access
A Facile Synthesis of Fully Protected meso-Diaminopimelic Acid (DAP) and Its Application to the Preparation of Lipophilic N-Acyl iE-DAP
18
Citations
29
References
2013
Year
Bioorganic ChemistryFacile SynthesisGlycobiologyImmunologyLipophilic N-acyl Ie-dapAllyl Glycine 2Cross MetathesisSynthetic ImmunologyMedicinal ChemistryGlycosylationMeso-dap 9BiochemistryBioconjugationNatural Product SynthesisPharmacologyBiomolecular EngineeringLipid PreparationNatural SciencesMedicineSynthetic Chemistry
Synthesis of beneficial protected meso-DAP 9 by cross metathesis of the Garner aldehyde-derived vinyl glycine 1b with protected allyl glycine 2 in the presence of Grubbs second-generation catalyst was performed. Preparation of lipophilic N-acyl iE-DAP as potent agonists of NOD 1-mediated immune response from 9 is described.
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