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Glycine synthesis and

These two selectors terminated with a glycine were then prepared on a larger scale, their carboxyl groups reacted with 3-aminopropyltriethoxysilane, and the conjugate immobilized onto silica. Each CSP was packed into columns and used for the separation of racemic (l-naphthyl)leucine ester 17. Separation factors of 6.9 and 8.0 were determined for the columns with DNB-ala-gly and DNB-leu-gly selector respectively. These were somewhat lower than those found for similar CSPs using the parallel synthesis and attached through a different tether [87]. [Pg.85]

The imines of ( )-(l/ ,2/ ,5/ )-2-hydroxy-3-pinanone and glycine, alanine and norvaline methyl esters were highly successful as Michael donors in the asymmetric synthesis of 2,3-di-substituted glutamates. The chiral azaallyl anions derived from these imines by deprotonation with lithium diisopropylamide in THF at — 80 "C undergo addition to various ,/ -unsaturated esters with modest to high diastereoselectivities210,394. [Pg.980]

Creatinine is formed in muscle from creatine phosphate by irreversible, nonenzymatic dehydration and loss of phosphate (Figure 31-6). The 24-hour urinary excretion of creatinine is proportionate to muscle mass. Glycine, arginine, and methionine all participate in creatine biosynthesis. Synthesis of creatine is completed by methylation of guanidoacetate by S-adenosylmethio-nine (Figure 31-6). [Pg.267]

Verleysdonk, S, Martin, H, Willker, W, Leibfritz, D and Hamprecht, B (1999) Rapid uptake and degradation of glycine by astroglial cells in culture synthesis and release of serine and lactate. Glia 27 239-248. [Pg.250]

GLYCINE AS A CENTRAL NEUROTRANSMITTER GLYCINE SYNTHESIS, UPTAKE AND DEGRADATION 298... [Pg.291]

The underlying biochemical defect is a failure of mitochondrial uptake of ornithine. This results in a failure of citrulline synthesis and a consequent hyperammonemia. Urinary orotic acid is high, presumably because of underutilization of carbamyl phosphate. In contrast, excretion of creatine is low, reflecting the inhibition of glycine trans-amidinase by excessive levels of ornithine. [Pg.680]

Ashton, W.T., Dong, H., Sisco, R.M., Doss, G.A., Leiting, B., Patel, R.A., Wu, J.K., Marsilio, F., Thornberry, N.A. and Weber, A.E. (2004) Diastereoselective synthesis and configuration-dependent activity of (3-substituted-cycloalkyl) glycine pyrrolidides and fhiazolidides as dipeptidyl peptidase IV inhibitors. Bioorganic at Medicinal Chemistry Letters, 14, 859-863. [Pg.421]

The amino acids glycine, aspartate, and glutamine are used in purine synthesis. [Pg.268]

They are required for the synthesis of conditionally essential amino acids, e.g. arginine, glycine, cysteine and glutamine. [Pg.423]

Researchers at the University of Graz, in collaboration with scientists from DSM, have developed an elegant and novel approach to the synthesis of P-amino alcohols using two different enzymes in one pot (Scheme 2.35). For example, a threonine aldolase-catalyzed reaction was initially used, under reversible conditions, to prepare L-70 from glycine 69 and benzaldehyde 68. L-70 was then converted to (R)-71 by an irreversible decarboxylation catalyzed by L-tyrosine decarboxylase. In a second example, D/L-syn-70 was converted to (R)-71 using the two enzymes shown combined with a D-threonine aldolase in greater than 99% e. e. and 67% yield ]37, 38]. [Pg.37]

Gershoff, S. N., and Earagalla, E. F. (1959). Endogenous oxalate synthesis and glycine, serine, deoxypyridoxine interrelationships in vitamin B6-deficient rats. /. Biol. Chem. 234, 2391-2393. [Pg.334]


See other pages where Glycine synthesis and is mentioned: [Pg.324]    [Pg.324]    [Pg.76]    [Pg.130]    [Pg.1119]    [Pg.156]    [Pg.193]    [Pg.238]    [Pg.246]    [Pg.150]    [Pg.243]    [Pg.90]    [Pg.196]    [Pg.229]    [Pg.63]    [Pg.201]    [Pg.142]    [Pg.240]    [Pg.1168]    [Pg.498]    [Pg.75]    [Pg.48]    [Pg.52]    [Pg.326]    [Pg.58]    [Pg.312]    [Pg.772]    [Pg.508]   


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Glycine synthesis

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