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Efficient enantioselective synthesis of orthogonally protected (R)-α-alkylserines compatible with the solid phase peptide synthesis
Authors:Stamatia Vassiliou  Plato A Magriotis
Institution:a Department of Chemistry, Laboratory of Organic Chemistry, University of Athens, Panepistimiopolis Zografou, 15771 Athens, Greece
b Department of Chemistry, New York University, 110 Washington Square East, New York, NY 10003, USA
Abstract:The Schöllkopf methodology for the asymmetric synthesis of α-amino acids, which was previously not applicable to the construction of quaternary α-amino acids, has been rendered not only suitable but also practical for this purpose and applied to a highly efficient enantioselective synthesis of orthogonally protected (R)-α-alkylserines suitable for the solid phase synthesis.
Keywords:α  α-Disubstituted α-amino acids  Quaternary α-amino acids  (R)-α-Alkylserines  Schö  llkopf methodology  tert-BuLi
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