Relevant bibliographies by topics / Deoxy

Academic literature on the topic 'Deoxy'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Deoxy"

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De Bruyn, A., and M. Anteunis. "1H NMR Study of 2-Deoxy-D-Arabino-Hexopyranose (2-Deoxy Glucopyranose), 2-Deoxy-D-Lyxo-Hexopyranose (2-Deoxy Galactopyranose) and 2′-Deoxy Lactose. Shift Increment Studies in 2-Deoxy Carbohydrates." Bulletin des Sociétés Chimiques Belges 84, no. 12 (September 1, 2010): 1201–9. http://dx.doi.org/10.1002/bscb.19750841208.

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Krečmerová, Marcela, Hubert Hřebabecký, Milena Masojídková, and Antonín Holý. "Preparation of Purine 2'-Deoxy-5'-O-phosphonomethylnucleosides and 2'-Deoxy-3'-O-phosphonomethylnucleosides." Collection of Czechoslovak Chemical Communications 58, no. 2 (1993): 421–34. http://dx.doi.org/10.1135/cccc19930421.

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Sodium salt of 2'-deoxy-N6-dimethylaminomethylene-3'-O-(tetrahydro-2H-pyran-2-yl)adenosine (VIII) reacted with dibenzyl p-toluenesulfonyloxymethanephosphonate (Ia) to give dibenzyl ester of 2'-deoxy-N6-dimethylaminomethylene-5'-O-phosphonomethyl-3'-O-(tetrahydro-2H-pyran-2-yl)adenosine (XI) which after deprotection afforded the final 2'-deoxy-5'-O-phosphonomethyladenosine (XII). 2'-Deoxy-5'-O-hydroxymethanephosphonyladenosine (XIV) and 5'-O-benzyloxymethanephosphonyl-2'-deoxyadenosine (XIII) were isolated as a side product. The preparation of 2'-deoxy-5'-O-phosphonomethylguanosine (XVI) and protection of the starting nucleoside were analogous to those of compound XII. In the 2'-deoxy-3'-O-phosphonomethylnucleosides series, 2'-deoxy-3'-O-phosphonomethylcytidine (XXI) and 2'-deoxy-3'-O-phosphonomethyladenosine (XXVII) were prepared, using N4-benzoyl-5'-O-tert-butyldiphenylsilyl-2'-deoxycytidine (XVIII) and 5'-O-tert-butyldiphenylsilyl-2'-deoxy-N6-dimethylaminomethyleneadenosine (XXIV), respectively, as starting compounds.
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Ledvina, Miroslav, Daniel Zyka, Jan Ježek, Tomáš Trnka, and David Šaman. "New Effective Synthesis of (N-Acetyl- and N-Stearoyl-2-amino-2-deoxy-β-D-glucopyranosyl)-(1→4)-N-acetylnormuramoyl-L-2-aminobutanoyl-D-isoglutamine, Analogs of GMDP with Immunopotentiating Activity." Collection of Czechoslovak Chemical Communications 63, no. 4 (1998): 577–89. http://dx.doi.org/10.1135/cccc19980577.

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Ethyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (5), prepared by benzylation of ethyl 2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside (4), was transformed by reaction with bromine into 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide (6). Thioglycoside 5 in the presence of methyl triflate and glycosylbromide 6 in the presence of silver triflate were used as glycosyl donors for condensation with benzyl 2-acetamido-3-O-allyl-6-O-benzyl-2-deoxy-α-D-glucopyranoside (7), to give benzyl 2-acetamido-3-O-allyl-6-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-2-deoxy-α-D-glucopyranoside (8). Its reductive dephthaloylation with NaBH4/AcOH afforded benzyl 2-acetamido-3-O-allyl-4-O-(2-amino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)- 6-O-benzyl-2-deoxy-α-D-glucopyranoside (11). Compound 11 was N-acylated to give benzyl 2-acetamido-4-O-(2-acylamino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-3-O-allyl-6-O-benzyl-2-deoxy-α-D-glucopyranosides (12a) or (12b). These compounds were converted into corresponding benzyl 2-acetamido-4-O-(2-acylamino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl)-6-O-benzyl-3-O-carboxymethyl-2-deoxy-α-D-glucopyranosides which, by condensation with H-L-Abu-D-isoGln(OBzl) followed by hydrogenolysis of protective benzyl groups, furnished glycopeptides 16a and 16b. Intramolecular O→N migration of the allyl protecting group followed by its reduction to the propyl residue by reaction of compound 8 with hydrazine or hydrazinium acetate, to give benzyl 2-acetamido-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-propylamino-β-D-glucopyranosyl)-6-O-benzyl-2-deoxy-α-D-glucopyranoside (9), is also described.
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Kefurt, Karel, Zdeňka Kefurtová, Věra Marková, and Karla Slívová. "Synthesis of 5-Amino-5-deoxypentonolactams." Collection of Czechoslovak Chemical Communications 61, no. 7 (1996): 1027–36. http://dx.doi.org/10.1135/cccc19961027.

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5-Azido-5-deoxy-1,2-O-isopropylidene-α-D-xylofuranose (4) and 5-azido-5-deoxy-1,2-O-isopropylidene-β-D-arabinofuranose (10) were prepared starting from D-xylose and D-arabinose, respectively. Using the oxidation-reduction way for the C-3 epimerization, 5-azido-5-deoxy-1,2-O-isopropylidene-α-D-ribofuranose (15) and 5-azido-5-deoxy-1,2-O-isopropylidene-β-D-lyxofuranose (17) were obtained from 4 and 10, respectively. The derivatives 4, 10, 15 and 17 afforded by acid hydrolysis, oxidation with bromine and catalytic hydrogenation successively the corresponding 5-azido-5-deoxy-D-pentofuranoses 6, 11, 18, 19, 5-azido-5-deoxy-D-pentonolactones 7, 12, 20, 21 and 5-amino-5-deoxy-D-pentonolactams 8, 13, 22, 23.
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Kennedy, Isaac A., Thomas Hemscheidt, James F. Britten, and Ian D. Spenser. "1-Deoxy-D-xylulose." Canadian Journal of Chemistry 73, no. 8 (August 1, 1995): 1329–37. http://dx.doi.org/10.1139/v95-164.

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1-Deoxy-D-xylulose (= 1-deoxy-D-theropentulose) is a precursor of thiamin (Vitamin B1) and of pyridoxine (Vitamin B6) in bacteria. The synthesis of a [2,3-13C2] bond-labeled sample of the compound, to be used for investigations of the biosynthesis of the two vitamins, is described. In aqueous solution 1-deoxy-D-xylulose exists mainly as the open chain ketone. In methanol solution the compound exists as a mixture of the open chain ketone and the two corresponding epimeric furanoses. In acid solution the compound yields a dimeric anhydride, di-β-1-deoxy-D-xylulofuranose 2,3′:3,2′-dianhydride, whose structure was established by X-ray crystallography. Keywords: [2,3-13C2]-1-deoxy-D-xylulose, di-β-1-deoxy-D-xylulofuranose 2,3′:3,2′-dianhydride, 5-O-benzyl-3,4-O-isopropylidene-1-deoxy-D-xylulose, 4-O-benzyl-2,3-O-isoproylidene-D-threose.
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Kato, N., F. Li, A. Mori, H. Takeshita, and T. Sassa. "9-Deoxy-15-hydroxy- and 9-Deoxy-19-hydroxycotylenol." Acta Crystallographica Section C Crystal Structure Communications 54, no. 8 (August 15, 1998): 1165–68. http://dx.doi.org/10.1107/s010827019800256x.

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Ibragimova, A. Sh, N. A. Ves’kina, I. V. Galyautdinov, and V. N. Odinokov. "Δ8(14)-14α-deoxy- and 14α-deoxy-14α-hydroperoxyecdysteroids." Russian Journal of Organic Chemistry 46, no. 11 (November 2010): 1735–40. http://dx.doi.org/10.1134/s1070428010110205.

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Ueno, Katsuhito, Shinichi Takamoto, Takeshi Miyairi, Tetsuro Morota, Ko Shibata, Arata Murakami, and Yutaka Kotsuka. "Multichannel Monitoring of Cerebral Circulatory and Oxygenation Status Using Optical Topography during Deep Hypothermic Retrograde Cerebral Perfusion." Vascular 12, no. 5 (September 2004): 325–30. http://dx.doi.org/10.1258/rsmvasc.12.5.325.

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In this study, we evaluated changes in the cerebral circulatory and oxygenation status during deep hypothermic total circulatory arrest (TCA) and retrograde cerebral perfusion (RCP) using optical topography, a form of multichannel near-infrared spectrophotometry, to monitor the broad area perfused by the middle cerebral artery. Seven patients underwent thoracic aortic surgery with TCA and RCP via the superior vena cava. Pressure-regulated RCP was performed under pH-stat. No postoperative neurologic complications occurred. Using optical topography, the relative changes in oxy-, deoxy-, and total hemoglobin (oxy-Hb, deoxy-Hb, total Hb) were simultaneously measured from 24 points in both hemispheres. Deoxy-Hb was used for evaluating the regional oxygenation status under RCP. The values of deoxy-Hb at the beginning of RCP were regarded as the basal values, and the rate of increase in deoxy-Hb per minute was calculated at each site. Deoxy-Hb/min during TCA was also calculated. In every case, both oxy-Hb and total Hb decreased and deoxy-Hb increased during TCA. When RCP was initiated, the decrease in oxy-Hb and the increase in deoxy-Hb were attenuated. The deoxy-Hb/min was significantly lower under RCP than during TCA in all portions. There was no significant difference of deoxy-Hb/min between any portions during RCP. Our results showed that the status of circulation and oxygenation might be uniform in the brain during RCP and better than that under TCA.
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Best, Wayne M., Robert V. Stick, and D. Matthew G. Tilbrook. "The Synthesis of Some Epoxyalkyl Deoxyhalo-β-cellobiosides." Australian Journal of Chemistry 50, no. 1 (1997): 13. http://dx.doi.org/10.1071/c96078.

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2,3-Epoxypropyl and 3,4-epoxybutyl 6′-deoxy-6′-iodo-β-cellobioside, together with 3,4-epoxybutyl 6′- deoxy-6′-fluoro-β-cellobioside, were prepared as putative inhibitors and reporter groups for events occurring at the active site of some β-glucan hydrolases. As well, related syntheses gave the previously unknown 6-deoxy-6-fluoro- and 6′-deoxy-6′-fluoro-cellobioses.
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Ledvina, Miroslav, Jiří Farkaš, Jaroslav Zajíček, Jan Ježek, and Milan Zaoral. "An alternative synthesis of O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)-N-acetylnormuramoyl-L-α-aminobutanoyl-D-isoglutamine." Collection of Czechoslovak Chemical Communications 54, no. 10 (1989): 2784–94. http://dx.doi.org/10.1135/cccc19892784.

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Silver triflate-promoted condensation of 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide (VIII) with benzyl 2-acetamido-6-O-benzoyl-2-deoxy-3-O-(methoxycarbonyl)-methyl-α-D-glucopyranoside (IV) afforded benzyl 2-acetamido-4-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-6-O-benzoyl-2-deoxy-3-O-(methoxycarbonyl)methyl-α-D-glucopyranoside (IX) which, after deprotection, was converted into the acid XI. Condensation of acid XI with L-α-aminobutanoyl-D-isoglutamine benzyl ester and subsequent hydrogenolysis of the product XIII furnished compound XIV. Benzyl 2-acetamido-6-O-benzoyl-2-deoxy-3-O-(methoxycarbonyl)methyl-α-D-glucopyranoside (IV) was prepared by partial benzoylation of benzyl 2-acetamido-2-deoxy-3-O-(methoxycarbonyl)methyl-α-D-glucopyranoside (III) with benzoyl cyanide.
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Dissertations / Theses on the topic "Deoxy"

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Roig, Ricard. "Synthesis of 6-deoxy-6-fluorosugars." Thesis, University of Leicester, 2006. http://hdl.handle.net/2381/29987.

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This project is based on the chemical synthesis of fluorosaccharide end-products, which could be used potentially as substrates for the combinatorial biosynthesis of novel complex structures like antibiotics. Although fluorine is the most abundant halogen in the earth's crust, the incidence of fluorinated natural products is extremely low. There are no examples of fluorosaccharide end-product molecules in nature, so novel architecture will result from their incorporation within oligosaccharides or complex antibiotics. Introducing fluorine into pharmaceutical compounds can increase the biological activity and stability to metabolism. Enantiomerically enriched and racemic 6-fluoro and racemic 6,6-difluoro analogues of amicetose and rhodinose have been synthesized successfully using different and scaleable strategies from commercially available starting materials. The equilibria between furanoses and pyranoses favoures the smaller rings, due to the inductive electron withdrawing effects of fluorine, so it was necessary to use protection to deliver pyranoses exclusively. Two very efficient new fluorinating methods have been developed, one with in situ cis/trans-isomerisation of a double bond with a mixture of TBAI and TBAF, and another one with high regioselective epoxides ring-opening with a mixture of KHF2 and TBAF. In addition to the synthesis of 6-deoxy-6-fluorosugars, a long lived difluoroenol was discovered and fully characterised, methanolysis rates and solvent isotope effect were measured.
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Park, Sung-Hae. "The biosynthesis of the deoxyhexose moieties in oleandomycin /." Thesis, Connect to this title online; UW restricted, 1999. http://hdl.handle.net/1773/8152.

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Sande, Marc van de. "Asymmetrische Synthese von 3-Oxa-15-Deoxy-16-(m-tolyl)-Tetranorisocarbacyclin und 15-Deoxy-16-(m-tolyl)-Tetranorisocarbacyclin." Aachen Mainz, 2007. http://d-nb.info/100174103X/34.

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Fazio, Fabio. "Building blocks for 2-deoxy-L-nucleosides." [S.l. : s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=963273434.

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Jiao, Hailong. "Synthetic studies on 2-amino-2-deoxy glycosides." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0002/NQ39546.pdf.

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Ellenberger, Suzanne Ray. "Total synthesis of selected deoxyamino sugars /." Full text open access at:, 1986. http://content.ohsu.edu/u?/etd,110.

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Sande, Marc van de [Verfasser]. "Asymmetrische Synthese von 3-Oxa-15-Deoxy-16-(m-tolyl)-Tetranorisocarbacyclin und 15-Deoxy-16-(m-tolyl)-Tetranorisocarbacyclin / vorgelegt von Marc van de Sande." Aachen : Mainz, 2007. http://d-nb.info/100174103X/34.

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Heß, David. "Palladium(II) complexes and phenylboronic acid esters of deoxy sugars." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-151675.

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Hardy, Simon. "Approaches towards the total synthesis of the 20-deoxy bryostatins." Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496225.

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This thesis describes approaches towards the total synthesis of the 20-deoxy bryostatins. The use of CI9 acyl anion equivalents as a means of forming the C19-C20 bond was investigated, leading to the synthesis of 2-[(2'E,6'Z)-(R)-6'-(2-benzyloxymethoxy-ethyl)-1', 1' -dimethyl-4' -triethylsilyloxy-8' -triisopropylsilyloxyocta-2',6'-dienyl]-[l,3]-dithiane (276), representing the C11-CI9 fragment of the bryostatatins.
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Steer, Andrew Mark. "Studies on the prebiotic origin of 2-deoxy-D-ribose." Thesis, University of York, 2017. http://etheses.whiterose.ac.uk/19070/.

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This research attempts to provide a possible explanation to the chemical origin of 2-deoxy-D-ribose via an aldol reaction of acetaldehyde and D-glyceraldehyde. The sugar mixture is trapped with N,N-diphenylhydrazine for ease of purification and characterisation. The reaction is promoted by amino acids, amino esters and amino nitriles consistently giving selectivities in favour of 2-deoxy-D-ribose. This is the first example of an amino nitrile-promoted reaction. The research is developed further by exploring the formation of 2-deoxy-D-ribose in a "protocell" environment - a primitive cell. Here we suggest that primitive cells may have been simple hydrogel systems. A discussion of the characterisation and catalytic ability of small peptide-based structures is included.
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Books on the topic "Deoxy"

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MacCulloch, Alasdair Cunningham. The synthesis and properties of novel 2'-deoxy-4'-thionucleoside analogues. Birmingham: University of Birmingham, 1997.

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Hotta, S. Steven. p18sF-labeled 2-deoxy-2-fluoro-D-glucose positron-emission tomography scans for the localization of the epileptogenic foci. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1998.

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Hotta, S. Steven. p18sF-labeled 2-deoxy-2-fluoro-D-glucose positron-emission tomography scans for the localization of the epileptogenic foci. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1998.

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Hotta, S. Steven. p18sF-labeled 2-deoxy-2-fluoro-D-glucose positron-emission tomography scans for the localization of the epileptogenic foci. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1998.

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Tracey, West. Destiny Deoxys. New York: Scholastic, 2005.

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Tracey, West. Pokémon: Battle frontier : Deoxys in danger ; Pokémon : Battle frontier : Grovyle trouble. New York: Scholastic, 2008.

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Rembold, Hansjörg. Die Anomere O-Alkylierung zur Synthese eines KDO (3-Desoxy-D-manno-2-octulosonsäure)-haltigen Lipid A-Analogen. Konstanz: Hartung-Gorre, 1991.

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Enhsen, Alfons. Synthese von 3-Desoxy-2-octulosonsäure (KDO) und Untersuchungen zur Synthese von N-Acetylneuraminsäure (NANA) aus funktionell substituierten Acrylsäurederivaten. Konstanz: Hartung-Gorre, 1988.

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Parker, Ricardo Jerome. Monoclonal antibodies to 5'-deoxy-5' methylthioadenosine phosphorylase. 1986.

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Rohr, J. Bioorganic Chemistry: Deoxysugars, Polyketides and Related Classes: Synthesis, Biosynthesis, Enzymes (Springer Desktop Editions in Chemistry). Springer, 2000.

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Book chapters on the topic "Deoxy"

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Gooch, Jan W. "Deoxy-." In Encyclopedic Dictionary of Polymers, 201. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3424.

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Schomburg, Dietmar, and Dörte Stephan. "(Deoxy)adenylate kinase." In Enzyme Handbook, 377–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_71.

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Schomburg, Dietmar, and Dörte Stephan. "3-Deoxy-2-octulosonidase." In Enzyme Handbook 15, 293–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-58948-5_66.

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Schomburg, Dietmar, and Dörte Stephan. "(Deoxy)nucleoside-phosphate kinase." In Enzyme Handbook, 385–88. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_73.

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Bennett, Clay S. "Selective Glycosylations with Deoxy Sugars." In Selective Glycosylations: Synthetic Methods and Catalysts, 277–95. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527696239.ch13.

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Schomburg, Dietmar, and Dörte Stephan. "3-Deoxy-manno-octulosonate cytidylyltransferase." In Enzyme Handbook, 661–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_119.

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Courtney, S. H., J. M. Friedman, R. G. Alden, M. D. Chavez, and M. R. Ondrias. "Vibrational Temperatures of Photoexcited Deoxy-Hemoglobin." In Springer Series in Chemical Physics, 538–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84269-6_163.

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Schomburg, Dietmar, and Margit Salzmann. "3-Deoxy-D-manno-octulosonate aldolase." In Enzyme Handbook 1, 361–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-86605-0_82.

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Schomburg, Dietmar, and Dörte Stephan. "2-Deoxy-D-gluconate 3-dehydrogenase." In Enzyme Handbook 9, 599–601. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-85200-8_120.

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Nukaga, Yohei, and Takeshi Wada. "Chemical Synthesis of Boranophosphate Deoxy-ribonucleotides." In Synthesis of Therapeutic Oligonucleotides, 271–84. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-1912-9_16.

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Conference papers on the topic "Deoxy"

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Machinami, Tomoya, Takashi Fujimoto, Yasuyuki Itaba, Ayumi Kayama, and Tetsuo Suami. "SYNTHESIS OF 7-DEOXY-N-ACETYLNEURAMINIC ACID DERIVATIVES VIA 2-AMINO-2-DEOXY-C-GLUCOSYL COMPOUNDS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.614.

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Van Calenbergh, Serge, Andreas Link, Shelly Fujikawa, Veerle Vanheusden, Denis De Keukeleire, Adriaan P. Ijzerman, and Piet Herdewijn. "5'-Deoxy congeners of 9-(3-amido-3-deoxy-β-D-xylofuranosyl)-N6-cyclopentyladenine: New adenosine A1 receptor antagonists." In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902273.

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Calado, Patrícia, Catarina Dias, Ana Marta Matos, Maria Teresa Blásquez-Sanchez, Alice Martins, Philipp Dätwyler, Beat Ernst, M. Paula Macedo, Nicola Colabufo, and Amélia Rauter. "Coupling deoxy sugars to polyphenols: Neuroprotection and bioavailability." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06341.

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Aidhen, Indrapal Singh, and Sivalenka Vijayasaradhi. "A SIMPLE APPROACH TOWARDS 2-DEOXY-C-ARYL PYRANOSIDES." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.573.

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Rausei, Magda. "Dynamic properties of deoxy hemoglobin encapsulated in silica gels." In Fifth scientific conference on nuclear and condensed matter physics. AIP, 2000. http://dx.doi.org/10.1063/1.1303365.

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Widyasari, Eva Maria, Auliya Nurasatidah Hudriyah, Witri Nuraeni, Teguh Hafiz Ambar Wibawa, and Maula Eka Sriyani. "Physicochemical characteristic of 99mTc-DTPA-deoxy-D-glucose radiopharmaceutical." In 2ND INTERNATIONAL CONFERENCE ON ENERGETICS, CIVIL AND AGRICULTURAL ENGINEERING 2021 (ICECAE 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0110202.

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Akula, Murthy, Derek Cressy, and Dustin Osborne. "Synthesis of N-acetamido-4-deoxy-4-[F-18]fluoroglucosamine." In RAD Conference. RAD Centre, 2022. http://dx.doi.org/10.21175/rad.sum.abstr.book.2022.26.3.

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Maki, Minna, Nina Jarvinen, Jarkko Rabina, Hannu Maaheimo, Leena Penttila, Pirkko Mattila, and Risto Renkonen. "BIOSYNTHESIS OF GDP-6-DEOXY-D-TALOSE IN ACTINOBACILLUS ACTINOMYCETEMCOMITANS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.699.

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Galpayage Dona, Kalpani Nisansala Udeni, Jia Liu, Yuhao Qiang, E. Du, and A. W. C. Lau. "Electrical Equivalent Circuit Model of Sickle Cell." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-70677.

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Abstract:
Mature red blood cell (RBC) consists of cytoplasm, mainly normal hemoglobin (HbA) within a plasma membrane. In sickle cell disease, abnormal sickle hemoglobin (HbS) molecule polymerizes and forms into rigid fibers at low oxygen tension, which contributes to variation in the biophysical properties of sickle cells from healthy RBCs. This paper presents an electrical equivalent circuit (EEC) model of sickle cell that considers the phase transition of oxy-HbS solution to deoxy-HbS polymers. Briefly, we model the oxy-HbS solution following healthy RBCs using a resistor and deoxy-HbS fibers as a capacitor. To validate the model, electrical impedance measurements of cell suspensions for normal RBCs and sickle cells are performed, using a multi-channel lock in amplifier in the frequency range of 1 kHz to 10 MHz in a customized microfluidic chamber. Quantitative measurements of the classical components of EEC model are extracted using the developed EEC sickle cell model, allowing us to better understand the biophysics of cell sickling event in sickle cell disease.
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Boryski, Jerzy, and Tomasz Zandecki. "Transglycosylation as a synthetic route towards 2'-deoxy-β-D-ribonucleosides." In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902242.

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Reports on the topic "Deoxy"

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Gilewski, Teresa A. Position Emitter I124 Iododeoxyuridine as a Tracer to Follow DNA Metabolism on Scans and in Tumor Samples in Advanced Breast Cancer: Comparison of 18F 2-Fluror-2-Deoxy-(D)-Glucose, as a Tracer for Glycolysis. Fort Belvoir, VA: Defense Technical Information Center, December 2005. http://dx.doi.org/10.21236/ada450668.

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