Literatura académica sobre el tema "Glycosyl hydroxylamines"
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Artículos de revistas sobre el tema "Glycosyl hydroxylamines"
Merino, P., S. Franco, F. L. Merchan y T. Tejero. "A Facile Synthesis of Glycosyl Hydroxylamines". Synthetic Communications 27, n.º 20 (1 de octubre de 1997): 3529–37. http://dx.doi.org/10.1080/00397919708007074.
Texto completoMERINO, P., S. FRANCO, F. L. MERCHAN y T. TEJERO. "ChemInform Abstract: A Facile Synthesis of Glycosyl Hydroxylamines". ChemInform 29, n.º 1 (24 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199801229.
Texto completoNimpaiboon, Adun, Sureerut Amnuaypornsri y Jitladda T. Sakdapipanich. "OBSTRUCTION OF STORAGE HARDENING IN NR BY USING POLAR CHEMICALS". Rubber Chemistry and Technology 89, n.º 2 (1 de junio de 2016): 358–68. http://dx.doi.org/10.5254/rct.16.84825.
Texto completoKuryanov, V. O., A. A. Luschtshyk y 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, n.º 4 (julio de 2013): 426–33. http://dx.doi.org/10.1134/s1068162013030084.
Texto completoReihani, Neda y 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, n.º 8 (28 de abril de 2021): 950–62. http://dx.doi.org/10.2174/1385272825666210212120517.
Texto completoDietl, Andreas, Wouter Maalcke y Thomas R. M. Barends. "An unexpected reactivity of the P460cofactor in hydroxylamine oxidoreductase". Acta Crystallographica Section D Biological Crystallography 71, n.º 8 (31 de julio de 2015): 1708–13. http://dx.doi.org/10.1107/s1399004715010706.
Texto completoPesyan, Nader Noroozi, Narmin Akhteh, Hana Batmani, Barış Anıl y 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, n.º 1 (10 de marzo de 2020): 26–32. http://dx.doi.org/10.1515/hc-2020-0005.
Texto completoLOPEZ-CAMACHO, Cristina, Jesus SALGADO, Juan Luis LEQUERICA, Alejo MADARRO, Esteban BALLESTAR, Luis FRANCO y Julio POLAINA. "Amino acid substitutions enhancing thermostability of Bacillus polymyxa β-glucosidase A". Biochemical Journal 314, n.º 3 (15 de marzo de 1996): 833–38. http://dx.doi.org/10.1042/bj3140833.
Texto completoQiu, Quan-Sheng y Nan Zhang. "Water stress inhibits p-nitrophenyl phosphate hydrolysis activity of the plasma membrane H+-ATPase from soybean hypocotyls". Functional Plant Biology 27, n.º 7 (2000): 717. http://dx.doi.org/10.1071/pp00017.
Texto completoShenoy-Scaria, A. M., D. J. Dietzen, J. Kwong, D. C. Link y D. M. Lublin. "Cysteine3 of Src family protein tyrosine kinase determines palmitoylation and localization in caveolae." Journal of Cell Biology 126, n.º 2 (15 de julio de 1994): 353–63. http://dx.doi.org/10.1083/jcb.126.2.353.
Texto completoTesis sobre el tema "Glycosyl hydroxylamines"
Talan, Rommel S. "Chemical Ligation of Glycopeptides". University of Toledo / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1278958947.
Texto completoMarradi, Marco. "New chiral nitrones for stereoselective syntheses of biologically active natural products and their analogues". Doctoral thesis, 2005. http://hdl.handle.net/2158/1161177.
Texto completoCapítulos de libros sobre el tema "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." En 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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