Publication | Open Access
Chemical Dynamic Thermodynamic Resolution and <i>S</i>/<i>R</i> Interconversion of Unprotected Unnatural Tailor-made α-Amino Acids
33
Citations
42
References
2015
Year
Bioorganic ChemistryMolecular BiologyOrganic ChemistryPeptide ScienceChemistryProtein FoldingStereoselective SynthesisCorresponding NickelProtein ChemistryBiochemistryDiversity-oriented SynthesisAsymmetric CatalysisEnantioselective SynthesisIntermediate FormationNatural SciencesPeptide SynthesisProtein EngineeringMedicineSchiff Bases
Described here is an advanced, general method for purely chemical dynamic thermodynamic resolution and S/R interconversion of unprotected tailor-made α-amino acids (α-AAs) through intermediate formation of the corresponding nickel(II)-chelated Schiff bases. The method features virtually complete stereochemical outcome, broad substrate generality (35 examples), and operationally convenient conditions allowing for large-scale preparation of the target α-AAs in enantiomerically pure form. Furthermore, the new type of nonracemizable axially chiral ligands can be quantitatively recycled and reused, rendering the whole process economically and synthetically attractive.
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