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5- phenyl valeric acid

Proof of the premise was found in the cyclization 7 of a-benzyl- 5-phenyl-valeric acid (XIII) and of a-benzyiglutaric add (XV) which gave the hydrindone derivatives XIV and XVI, respectively, and none of the isomeric benzosuberones. The formation of 4-phenylhydrindone-l from /3-2-biphenylpropionic acid afforded further substantiation, since the acid has the structural possibility of cyclizing to a seven-membered ring ketone. ... [Pg.118]

The xylofuranose-derived N-cinnamoyl oxazinone 2 0 reacts with two equivalents of diethylaluminium chloride to deliver the 3-phenyl-valeric acid derivative 21 in high yield (eq. 8). The stereoselection achieved so far is only moderate. A surprising feature of this new 1,4-addition to carboxylic acid derivatives is revealed, when other dialkylaluminium chlorides are used. [Pg.194]

Other cyclic tetrapeptides have also been isolated by Japanese workers and AM toxins I, II, and III, isolated from Alternaria mail., are extremely toxic to certain plant species (9.10). These are constructed of L- i-hydroxyisovaleric acid, L-alanine, c-amino-acrylic acid and, in AM toxin I, L-6(-amino- -( .-methoxyphenyl)-valeric acid. The phenyl residue in AM toxin II is L-t(-amino-S-phenylvaleric acid, while in AM toxin III, it is L-ol-amino-( .-hydroxyphenyl)valeric acid (Figure 2), All the AM toxins produce leaf spot, or necrosis, in apple but as might he expected slight change in substitution (R-group) on the phenyl ring radically alters the specific activity of the molecule. Both AM toxin I and III induce interveinal necrosis in the "Indo" apple cultivar, which is also highly susceptible to A. mail. at concentrations as low as 0.1 pph within 18 h after treatment. In contrast, the resistant apple cultivar "Jonathan" is only affected by 1 ppm of AM toxin I and 10 ppm of AM toxin III. [Pg.26]

Antagonists of biotin include desthiobiotin in some forms, ureylene phenyl, homobiotin, urelenecyclohexyl butync and valeric acid, norbiotin, avidin, lysolecithin. and biotin sulfone. Synergists indude vitamins B>. B6, B 2, folic acid, pantothenic add. somatotrophin (growth hormone), and testosterone. [Pg.236]

Figure 3.20. Analysis of carboxylic acids and alcohols by reversed phase HPLC, with indirect UV detection, (a) Carboxylic acids. Chromatography conditions mobile phase, 3 X 10 4 M l-phenethyl-2-picolinium in acetate buffer (pH 4.6) column, ju-Bondapak phenyl detection, indirect UV absorbance at 254 nm. Peaks 1, acetic acid 2, propionic acid 3, butyric acid 4, valeric acid 5, caproic acid S, system peak, (b) Aliphatic alcohols. Chromatography conditions mobile phase, 4 x 10 4 M nicotinamide in water column. Ultrasphere ODS detection, indirect UV absorbance at 268 nm. Peaks 1, methanol 2, propylene glycol 3, ethanol 4, 2-propanol 5, 1-propanol 6, system peak 7, 2-butanol 8, 2-methyl-l-propanol 9, 1-butanol. (Redrawn from Refs. 23 and 24 with permission.)... Figure 3.20. Analysis of carboxylic acids and alcohols by reversed phase HPLC, with indirect UV detection, (a) Carboxylic acids. Chromatography conditions mobile phase, 3 X 10 4 M l-phenethyl-2-picolinium in acetate buffer (pH 4.6) column, ju-Bondapak phenyl detection, indirect UV absorbance at 254 nm. Peaks 1, acetic acid 2, propionic acid 3, butyric acid 4, valeric acid 5, caproic acid S, system peak, (b) Aliphatic alcohols. Chromatography conditions mobile phase, 4 x 10 4 M nicotinamide in water column. Ultrasphere ODS detection, indirect UV absorbance at 268 nm. Peaks 1, methanol 2, propylene glycol 3, ethanol 4, 2-propanol 5, 1-propanol 6, system peak 7, 2-butanol 8, 2-methyl-l-propanol 9, 1-butanol. (Redrawn from Refs. 23 and 24 with permission.)...
FIGURE 57.11. Reaction of a serine esterase with phenyl valerate to yield phenol and valeric acid (Kayyali et al., 1991). [Pg.870]

NTE is an integral membrane protein in neurons and some non-neural cell types of vertebrates [3,27,32] and its activity depends on lipid contents. It is present in all neurons, but is absent from glia [32], NTE can hydrolyze many esters of carboxylic acids. NTE is conveniently detected in vitro by its ability to catalyse OP-sensitive hydrolysis of an artificial substrate, phenyl valerate. Its activity is operationally defined as phenyl valerate hydrolysis resistant to inhibition by 0,0-diethyl-4-nitrophenyl phosphate (paraoxon, non-neuropathic) and sensitive to inhibition by NJ T-diisopropyl phosphorodiamidic fluoride (mipafox, neuropathic), determined under specified conditions [3]. Differential centrifugation of brain homogenates resulted in an enrichment of NTE in microsomal fractions containing elements of endoplasmic reticulum (ER), Goldgi, and plasma membrane [39],... [Pg.278]

This compound is most easily named by treating the phenyl group as a substituent. The phenyl group is bonded to carbon-4 (or the y-carbon, in the common system of nomenclature). The parent compoimd is pentanoic acid (valeric acid in the common system). Hence the name of this compound is... [Pg.426]

Propylene glycol phenyl ether Sorbic acid Tetrachiorophthalic anhydride Tetradecene-1 Tetrahydrophthalic anhydride N,N,N, N -Tetramethylhexanediamine N,N,N, N -Tetramethyl-1,3-propanediamine Tripropylene glycol n-Valeric acid intermediate, plastics... [Pg.5408]


See other pages where 5- phenyl valeric acid is mentioned: [Pg.326]    [Pg.81]    [Pg.326]    [Pg.82]    [Pg.83]    [Pg.85]    [Pg.326]    [Pg.2155]    [Pg.81]    [Pg.69]    [Pg.293]    [Pg.45]    [Pg.2155]    [Pg.326]    [Pg.219]    [Pg.68]    [Pg.81]    [Pg.82]    [Pg.83]    [Pg.83]    [Pg.85]    [Pg.531]    [Pg.987]    [Pg.415]    [Pg.677]    [Pg.283]    [Pg.875]    [Pg.804]    [Pg.1416]    [Pg.572]    [Pg.290]    [Pg.259]    [Pg.176]    [Pg.764]    [Pg.764]    [Pg.464]    [Pg.395]    [Pg.657]    [Pg.638]    [Pg.560]    [Pg.322]   
See also in sourсe #XX -- [ Pg.81 ]




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5- valeric acid

Phenyl valerate

Phenylic acid

Valeral

Valerate

Valerates

Valeric

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