83537-81-9Relevant articles and documents
Efficient enantioselective synthesis of orthogonally protected (R)-α-alkylserines compatible with the solid phase peptide synthesis
Vassiliou, Stamatia,Yiotakis, Athanasios,Magriotis, Plato A.
, p. 7339 - 7341 (2007/10/03)
The Sch?llkopf 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.
Asymmetric Syntheses via Heterocyclic Intermediates, XI Enantioselective Synthesis of (R)-(-)-α-Methylserine
Groth, Ulrich,Chiang, Yao-chung,Schoellkopf, Ulrich
, p. 1756 - 1757 (2007/10/02)
Die Titelverbindung 7 wurde in enantiomerenreiner Form durch asymmetrische Synthese dargestellt unter Verwendung des Bislyctimethers 1 von cyclo-(L-Val-DL-Ala) als Ausgangsverbindung.
