Organic & Biomolecular Chemistry · 2011 · 13 citations · 44 references
PharmacyChemistryMedicinal ChemistryDrug DiscoverySynthetic Medicinal ChemistryAmino Acid ChemistryLigand BindingMacrocycle SynthesisPeptidomimetic DesignProtecting-group StrategyReceptor-ligand InteractionsAmino Acid Protection ChemistryChemoselective CouplingChemoselective FunctionalizationChemoselective Library SynthesisChemoselective SynthesisPeptide Medicinal ChemistryProtecting Group ChemistryProtecting Group-free Synthesis
In our pursuit of an efficient, protecting-group-free synthesis of the dual CCK1/CCK2 receptor antagonist 1, we have developed chemoselective conditions for sulfonamide formation reaction in pure water and a PhNMe(2) mediated carboxamide formation, both in the presence of a carboxylic acid. Practical synthesis of an unnatural, chiral β-aryl-α-amino acid is also described.
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Asymmetric Hydrogenations (Nobel Lecture 2001)
William S. Knowles · Advanced Synthesis & Catalysis · 2003 · 943 citations
Mark J. Burk, John E. Feaster, William A. Nugent et al. · Journal of the American Chemical Society · 1993 · 602 citations