Relevant bibliographies by topics / Valeronitrile

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Academic literature on the topic 'Valeronitrile'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Valeronitrile"

1

Sarlea, Michael, Sabine Kohl, Nina Blickhan, and Herbert Vogel. "Valeronitrile Hydrolysis in Supercritical Water." ChemSusChem 3, no. 1 (January 25, 2010): 85–90. http://dx.doi.org/10.1002/cssc.200900154.

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Sarlea, Michael, Sabine Kohl, Nina Blickhan, and Herbert Vogel. "Homogeneous Catalysis of Valeronitrile Hydrolysis under Supercritical Conditions." ChemSusChem 5, no. 1 (December 20, 2011): 200–205. http://dx.doi.org/10.1002/cssc.201100443.

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Jiao, Yunzhe, William W. Brennessel, and William D. Jones. "Nitrile coordination to rhodium does not lead to C—H activation." Acta Crystallographica Section C Structural Chemistry 72, no. 11 (October 5, 2016): 850–52. http://dx.doi.org/10.1107/s2053229616006859.

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Tris(pyrazolyl)borate complexes of rhodium are well known to activate C—H bonds. The reactive [Tp′Rh(PMe3)] fragment [Tp′ is tris(3,5-dimethylpyrazol-1-yl)hydroborate] is found to react with valeronitrile to give the κ1N-bound complex (pentanenitrile-κN)(trimethylphosphane-κP)[tris(3,5-dimethylimidazol-1-yl)hydroborato-κ2N2,N2′]rhodium(I), [Rh(C15H22BN6)(C5H9N)(C3H9P)]. In contrast to the widespread evidence for the reaction of this fragment with C—H bondsviaoxidative addition, no evidence for such a complex is observed.
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Butora, Gabriel, Ludvík Bláha, Miroslav Rajšner, and Ivan Helfert. "Some New Analogues of Verapamil and Mepamil. Synthesis and Basic Pharmacological Properties." Collection of Czechoslovak Chemical Communications 57, no. 9 (1992): 1967–81. http://dx.doi.org/10.1135/cccc19921967.

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Some new analogues of verapamil (Ia) and mepamil (Ib), calcium antagonists of arylalkylamine type, were synthesized and screened for cardiovascular activities. The basic structure was modified a) on the phenyl ring, attached to the quaternary carbon, b) on the alkyl group, attached to the quaternary carbon and c) on the alkylamino group, attached in position 3 to the n-propyl fragment. Except of 2-(2-chlorophenyl)-2-isopropyl-5-(N-methylhomoveratrylamino)valeronitrile (VIa), all the synthesized compounds exhibited lower hypotensive activity, than the mother compound, verapamil.
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Bakac, Andreja, and James H. Espenson. "Facile cyclization of the valeronitrile group bound to a nickel macrocycle." Journal of the American Chemical Society 108, no. 17 (August 1986): 5353–54. http://dx.doi.org/10.1021/ja00277a055.

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Yang, Yi, and Yun-Ting Tsai. "Evaluation on the Photosensitivity of 2,2′-Azobis(2,4-Dimethyl)Valeronitrile with UV." Molecules 22, no. 12 (December 14, 2017): 2219. http://dx.doi.org/10.3390/molecules22122219.

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7

Neuhaus, Johannes, Erik von Harbou, and Hans Hasse. "Spectroscopic investigations of solutions of lithium bis(fluorosulfonyl) imide (LiFSI) in valeronitrile." Polyhedron 183 (June 2020): 114458. http://dx.doi.org/10.1016/j.poly.2020.114458.

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8

Shvedova, Anna A., Yulia Y. Tyurina, Vladimir A. Tyurina, Yoko Kikuchi, Valerian E. Kagan, and Peter J. Quinn. "Quantitative Analysis of Phospholipid Peroxidation and Antioxidant Protection in Live Human Epidermal Keratinocytes." Bioscience Reports 21, no. 1 (February 1, 2001): 33–43. http://dx.doi.org/10.1023/a:1010430000701.

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To characterize oxidative stress in phospholipids of normal human epidermal keratinocytes we metabolically labeled their membrane phospholipids with a natural oxidation-sensitive fluorescent fatty acid, cis-parinaric acid, and exposed the cells to two different sources of oxidants–a lipid-soluble azo-initiator of peroxyl radicals, 2,2′-azobis(2,4-dimethyl-valeronitrile), AMVN, and a superoxide generator, xanthine oxidase/xanthine. We demonstrated that both oxidants induced pronounced oxidation of four major classes of cis-parinaric acid-labeled phospholipids–phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, and phosphatidylinositol–in normal human epidermal keratinocytes that was not detectable as any significant change of their phospholipid composition. Vitamin E was effective in protecting the cells against phospholipid peroxidation. Since viability of normal human epidermal keratinocytes was not changed either by labeling or exposure to oxidants the labeling protocol and oxidative stress employed are compatible with the quantitative analysis of phospholipid peroxidation in viable cells.
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Neuhaus, Johannes, Erik von Harbou, and Hans Hasse. "Physico-Chemical Properties of LiFSI Solutions I. LiFSI with Valeronitrile, Dichloromethane, 1,2-Dichloroethane, and 1,2-Dichlorobenzene." Journal of Chemical & Engineering Data 64, no. 3 (February 6, 2019): 868–77. http://dx.doi.org/10.1021/acs.jced.8b00590.

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HATATE, YASUO, HIROSHI HAMADA, ATSUSHI IKARI, and FUMIYUKI NAKASHIO. "Styrene slurry polymerization within suspended droplets in water using 2,2'-azobis(2,4-dimethyl-valeronitrile) as initiator." Journal of Chemical Engineering of Japan 20, no. 6 (1987): 644–46. http://dx.doi.org/10.1252/jcej.20.644.

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Dissertations / Theses on the topic "Valeronitrile"

1

Costa, Sylvie. "Les nitriles : détection et dosage dans le sang, étude préliminaire chez les victimes d'incendie." Paris 5, 1990. http://www.theses.fr/1990PA05P115.

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Djaouadi, Djamal. "Réduction du valéronitrile en phase liquide sur des catalyseurs à base de nickel de Raney." Grenoble 1, 1993. http://www.theses.fr/1993GRE10006.

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La reduction catalytique en phase liquide du valeronitrile a ete etudiee sur nickel de raney dans le but d'obtenir selectivement l'amine primaire. L'effet de differents parametres de reaction sur la vitesse d'hydrogenation et la selectivite a ete examine et a permis de confirmer le reseau reactionnel complexe avec reversibilite des reactions. Des catalyseurs non dopes ou promus avec des elements metalliques (cr, fe, co, mo, ti. . . ) ont ete prepares a partir des phases metallurgiques ni#2al#3 ou nial#3. Les alliages et les catalyseurs ont ete caracterises par analyse chimique, stem-edx, xps, spectroscopie auger. . . Les dopants fer et chrome ameliorent l'activite et la selectivite du catalyseur, quel que soit l'alliage de depart, la reduction de la dipentylimine intermediaire sur ces memes catalyseurs a permis d'expliquer les ameliorations de selectivite observees en reduction du valeronitrile. L'adsorption du valeronitrile et de ses produits d'hydrogenation sur ces catalyseurs a ete effectuee en phase liquide. Le nitrile et l'amine s'adsorbent sur des sites differents; l'adsorption de valeronitrile est liee a la quantite d'hydrogene chimisorbe
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Book chapters on the topic "Valeronitrile"

1

Holze, Rudolf. "Ionic conductivities of valeronitrile." In Electrochemistry, 208. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_191.

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2

WANG, JUN-LAN, and DONALD R. BUHLER. "Valeronitrile." In Nitrogen and Phosphorus Solvents, 359–62. Elsevier, 1990. http://dx.doi.org/10.1016/b978-0-444-81316-9.50060-8.

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Besson, M., D. Djaouadi, J. M. Bonnier, S. Hamar-Thibault, and M. Joucla. "Structure and Catalytic Properties in Hydrogenation of Valeronitrile of Raney Nickel Prepared from Cr and Mo Doped Ni2Al3 Alloys." In Studies in Surface Science and Catalysis, 113–20. Elsevier, 1991. http://dx.doi.org/10.1016/s0167-2991(08)61111-8.

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You might also be interested in the extended bibliographies on the topic 'Valeronitrile' for particular source types:
Journal articles
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