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Asymmetric synthesis of organoelemental analogs of natural compounds. 7. (2R,3S)-2-amino-3-hydroxy-5-phosphonovaleric acid
Authors:V A Soloshonok  N Yu Svistunova  V P Kukhar'  A O Gudima  N A Kuz'mina  Yu N Belokon'
Abstract:The reaction of the Ni(II) complex of the Schiff base of glycine with (S)-2-N-(N1-benzylprolyl)-o-aminobenzophenone with diethyl-3-bromo-2-hydroxypropyl phosphonate yields the corresponding complex from which (2R, 3S)-2-amino-3-hydroxy-5-phosphonovaleric acid is separated with HCl.See 1] for Communication 6.Institute of Bioorganic Chemistry and Petrochemistry, Ukrainian Academy of Sciences, 252660 Kiev; N. A. Nesmeyanov Institute of Organoelemental Compounds, Russian Academy of Sciences, 117813 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 5, pp. 1172–1175, May, 1992.
Keywords:asymmetric synthesis  (S)-2-N-(N1-benzylprolyl)-o-aminobenzophenone  (2R  3S)-2-amino-3-hydroxy-5-phosphonovaleric acid
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