129849-32-7Relevant academic research and scientific papers
Synthesis of (R)-4-oxo-5-phosphononorvaline, an N-methyl-D-aspartic acid receptor selective β-keto phosphonate
Rudisill,Whitten
, p. 851 - 854 (1994)
(R)-4-Oxo-5-phosphononorvaline (1), a selective NMDA glutamate site antagonist, has been synthesized in four steps (overall yield = 31%) from (R)-aspartic acid, without racemization.
Design and Synthesis of &γ-Oxygenated Phosphinothricins as Inhibitors of Glutamine Synthetase
Walker, Daniel M.,McDonald, John F.,Franz, John E.,Logusch, Eugene W.
, p. 659 - 666 (2007/10/02)
The ability of L-γ-hydroxyglutamic acids to act as substrates of the enzyme glutamine synthetase (GS) was exploited as a rationale for the synthesis of γ-oxygenated analogues of the naturally occurring GS inhibitor phosphinothricin (PPT).The potent new in
Synthesis of N-(tert-Butoxycarbonyl)-3-(4-thiazolyl)-L-alanine
Hsiao, Chi-Nung,Leanna, M. Robert,Bhagavatula, Lakshmi,Lara, Edvin De,Zydowsky, Thomas M.,et al.
, p. 3507 - 3517 (2007/10/02)
Efficient syntheses of N-(tert-butoxycarbonyl)-3-(4-thiazolyl)-L-alanine (11) are described.
