Littérature scientifique sur le sujet « Glycosyl hydroxylamines »
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Articles de revues sur le sujet "Glycosyl hydroxylamines"
Merino, P., S. Franco, F. L. Merchan et T. Tejero. « A Facile Synthesis of Glycosyl Hydroxylamines ». Synthetic Communications 27, no 20 (1 octobre 1997) : 3529–37. http://dx.doi.org/10.1080/00397919708007074.
Texte intégralMERINO, P., S. FRANCO, F. L. MERCHAN et T. TEJERO. « ChemInform Abstract : A Facile Synthesis of Glycosyl Hydroxylamines ». ChemInform 29, no 1 (24 juin 2010) : no. http://dx.doi.org/10.1002/chin.199801229.
Texte intégralNimpaiboon, Adun, Sureerut Amnuaypornsri et Jitladda T. Sakdapipanich. « OBSTRUCTION OF STORAGE HARDENING IN NR BY USING POLAR CHEMICALS ». Rubber Chemistry and Technology 89, no 2 (1 juin 2016) : 358–68. http://dx.doi.org/10.5254/rct.16.84825.
Texte intégralKuryanov, V. O., A. A. Luschtshyk et T. A. Chupakhina. « Glycosylated derivatives of substituted hydroxylamine. II. The phase transfer synthesis and the study of the glycosyl transfer reaction of glucosaminides of substituted hydroxylamine ». Russian Journal of Bioorganic Chemistry 39, no 4 (juillet 2013) : 426–33. http://dx.doi.org/10.1134/s1068162013030084.
Texte intégralReihani, Neda, et Hamzeh Kiyani. « Three-component Synthesis of 4-Arylidene-3-alkylisoxazol-5(4H)-ones in the Presence of Potassium 2,5-dioxoimidazolidin-1-ide ». Current Organic Chemistry 25, no 8 (28 avril 2021) : 950–62. http://dx.doi.org/10.2174/1385272825666210212120517.
Texte intégralDietl, Andreas, Wouter Maalcke et Thomas R. M. Barends. « An unexpected reactivity of the P460cofactor in hydroxylamine oxidoreductase ». Acta Crystallographica Section D Biological Crystallography 71, no 8 (31 juillet 2015) : 1708–13. http://dx.doi.org/10.1107/s1399004715010706.
Texte intégralPesyan, Nader Noroozi, Narmin Akhteh, Hana Batmani, Barış Anıl et Ertan Şahin. « A Facile and Catalyst-free Synthesis of Hexahydroacridine-1,8(2H,5H )-dione and Octahydroacridin-10(1H )-yl)thiourea Derivatives : Inter- and Intramolecular Aza-Michael addition ». Heterocyclic Communications 26, no 1 (10 mars 2020) : 26–32. http://dx.doi.org/10.1515/hc-2020-0005.
Texte intégralLOPEZ-CAMACHO, Cristina, Jesus SALGADO, Juan Luis LEQUERICA, Alejo MADARRO, Esteban BALLESTAR, Luis FRANCO et Julio POLAINA. « Amino acid substitutions enhancing thermostability of Bacillus polymyxa β-glucosidase A ». Biochemical Journal 314, no 3 (15 mars 1996) : 833–38. http://dx.doi.org/10.1042/bj3140833.
Texte intégralQiu, Quan-Sheng, et Nan Zhang. « Water stress inhibits p-nitrophenyl phosphate hydrolysis activity of the plasma membrane H+-ATPase from soybean hypocotyls ». Functional Plant Biology 27, no 7 (2000) : 717. http://dx.doi.org/10.1071/pp00017.
Texte intégralShenoy-Scaria, A. M., D. J. Dietzen, J. Kwong, D. C. Link et D. M. Lublin. « Cysteine3 of Src family protein tyrosine kinase determines palmitoylation and localization in caveolae. » Journal of Cell Biology 126, no 2 (15 juillet 1994) : 353–63. http://dx.doi.org/10.1083/jcb.126.2.353.
Texte intégralThèses sur le sujet "Glycosyl hydroxylamines"
Talan, Rommel S. « Chemical Ligation of Glycopeptides ». University of Toledo / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1278958947.
Texte intégralMarradi, Marco. « New chiral nitrones for stereoselective syntheses of biologically active natural products and their analogues ». Doctoral thesis, 2005. http://hdl.handle.net/2158/1161177.
Texte intégralChapitres de livres sur le sujet "Glycosyl hydroxylamines"
« Samples of raw and treated slurry were centrifuged at 10,OOOg for 20 minutes at 10°C, as described by Hissett et al (25), to prepare the supernatants for the measurement of BOD. Determination. of. Total ..Organic A?ids, (TOA) TOA were determined, in the supernatant prepared as described by Hissett et al (25), by the method of Montgomery et al (26). The organic acids were esterified with acidified ethylene glycol. The esters were then reacted with hydroxylamine and the hydroxamic acids thus formed were converted to their ferric complexes and their concentrations were determined by optical density measurements at 500u. Gas-liauid Chromatography of VFA and TIP A Pye series 104 gas-liquid chromatograph (Pye Unicam Ltd.,Cambr idge,UK.) and a Packard model 439 gas-liquid chromatograph (Packard Instrument Ltd.,Reading,UK.) with a Hewlett Packard HP 3390A reporting integrator (Hewlett Packard Ltd.,Cheshire,UK.) were used. Determination of VFA were by direct injection of acidified supernatant samples into a 2.15 m long by 4mm ID packed column of 5% FFAP on Cnromosorb G.AW.DMCS 80/100 mesh. Determination of TIP were by direct injection of solvent extracts, of whole samples (30), into a 25 m long by 0.23 mm ID capillary column of WCOT fused Silica with liquid phase CP sil 5CB (United Technologies Packard,Reading,UK.). Odour Assessment The odour panel consisted of 21 College Staff who had previous odour panel experience (5) and 5 staff who were later recruited and whose performances at slurry odour assessments were judged to be similar to those of the original panellists. The method of assessment of odour offensiveness was based on that of Sobel (19). 20 ml samples of slurry were tranferred to 60 ml black glass bottles as described by Williams (5). These were handed to panellists in their own offices or laboratories where they were already accustomed to the background odour and were least hindered by interruption. The panellists were shown a copy of Table I and asked to assign the odour offensiveness of each sample to a value between 0 and 5. They were specifically requested not to consider the samples relative strength compared with the other samples. » Dans Odour Prevention and Control of Organic Sludge and Livestock Farming, 324. CRC Press, 1986. http://dx.doi.org/10.1201/9781482286311-121.
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