Статті в журналах з теми "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.
Повний текст джерелаKrečmerová, 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.
Повний текст джерелаLedvina, Miroslav, Daniel Zyka, Jan Ježek, Tomáš Trnka та 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, № 4 (1998): 577–89. http://dx.doi.org/10.1135/cccc19980577.
Повний текст джерелаKefurt, 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.
Повний текст джерелаKennedy, 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.
Повний текст джерелаKato, 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.
Повний текст джерелаIbragimova, A. Sh, N. A. Ves’kina, I. V. Galyautdinov та V. N. Odinokov. "Δ8(14)-14α-deoxy- and 14α-deoxy-14α-hydroperoxyecdysteroids". Russian Journal of Organic Chemistry 46, № 11 (листопад 2010): 1735–40. http://dx.doi.org/10.1134/s1070428010110205.
Повний текст джерелаUeno, 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.
Повний текст джерелаBest, Wayne M., Robert V. Stick та D. Matthew G. Tilbrook. "The Synthesis of Some Epoxyalkyl Deoxyhalo-β-cellobiosides". Australian Journal of Chemistry 50, № 1 (1997): 13. http://dx.doi.org/10.1071/c96078.
Повний текст джерелаLedvina, Miroslav, Jiří Farkaš, Jaroslav Zajíček, Jan Ježek та 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, № 10 (1989): 2784–94. http://dx.doi.org/10.1135/cccc19892784.
Повний текст джерелаLiu, Feng-Wu, Wenke Xu, Hui Yang, Yingju Liu, Yingchun Hua, Bin He, Xin Ning, Zhiyan Qin та Hong-Min Liu. "Facile Approaches to 2-Deoxy-d-glucose and 2-Deoxy-α-d-glucopyranonucleosides from d-Glucal". Synthesis 49, № 16 (7 червня 2017): 3686–91. http://dx.doi.org/10.1055/s-0036-1589501.
Повний текст джерелаZiemniak, Marcin, Sylwia Pawlędzio, Anna Zawadzka-Kaźmierczuk, Paulina M. Dominiak, Damian Trzybiński, Wiktor Koźmiński, Rafał Zieliński, et al. "X-ray wavefunction refinement and comprehensive structural studies on bromo-substituted analogues of 2-deoxy-d-glucose in solid state and solution." RSC Advances 12, no. 14 (2022): 8345–60. http://dx.doi.org/10.1039/d1ra08312k.
Повний текст джерелаVeselý, Jan, Miroslav Ledvina, Jindřich Jindřich, Tomáš Trnka та David Šaman. "Synthesis of 2-Amino-2-deoxy-β-D-galactopyranosyl-(1→4)-2-amino-2-deoxy-β-D-galactopyranosides: Using Various 2-Deoxy-2-phthalimido-D-galactopyranosyl Donors and Acceptors". Collection of Czechoslovak Chemical Communications 69, № 10 (2004): 1914–38. http://dx.doi.org/10.1135/cccc20041914.
Повний текст джерелаEl-Ghaouth, Ahmed, Joseph L. Smilanick, Michael Wisniewski, and Charles L. Wilson. "Improved Control of Apple and Citrus Fruit Decay with a Combination of Candida saitoana and 2-Deoxy-D-Glucose." Plant Disease 84, no. 3 (March 2000): 249–53. http://dx.doi.org/10.1094/pdis.2000.84.3.249.
Повний текст джерелаHigashimoto, Yuji, Noritsugu Honda, Toshiyuki Yamagata, Akiko Sano, Osamu Nishiyama, Hiroyuki Sano, Takashi Iwanaga, et al. "Exertional dyspnoea and cortical oxygenation in patients with COPD." European Respiratory Journal 46, no. 6 (October 22, 2015): 1615–24. http://dx.doi.org/10.1183/13993003.00541-2015.
Повний текст джерелаEl-Ghaouth, Ahmed, Charles L. Wilson, and Michael Wisniewski. "Antifungal Activity of 2-Deoxy-D-Glucose on Botrytis cinerea, Penicillium expansum, and Rhizopus stolonifer: Ultrastructural and Cytochemical Aspects." Phytopathology® 87, no. 7 (July 1997): 772–79. http://dx.doi.org/10.1094/phyto.1997.87.7.772.
Повний текст джерелаMedonos, Ivan, Věroslava Kocíková, Jan Staněk, Alena Zobáčová та Jiří Jarý. "Methyl esthers of methyl 2-deoxy-α- and β-D-threo-pentopyranoside". Collection of Czechoslovak Chemical Communications 51, № 8 (1986): 1671–77. http://dx.doi.org/10.1135/cccc19861671.
Повний текст джерелаJenkinson, Sarah F., K. Victoria Booth, Pushpakiran Gullapalli, Kenji Morimoto, Ken Izumori, George W. J. Fleet, and David J. Watkin. "1-Deoxy-L-mannitol (6-deoxy-L-mannitol orL-rhamnitol)." Acta Crystallographica Section E Structure Reports Online 64, no. 9 (August 6, 2008): o1705—o1706. http://dx.doi.org/10.1107/s1600536808024586.
Повний текст джерелаKazakova, Ekaterina D., Dmitry V. Yashunsky, Elena A. Khatuntseva, and Nikolay E. Nifantiev. "Azidophenylselenylation of glycals towards 2-azido-2-deoxy-selenoglycosides and their application in oligosaccharide synthesis." Pure and Applied Chemistry 92, no. 7 (July 28, 2020): 1047–56. http://dx.doi.org/10.1515/pac-2020-0105.
Повний текст джерелаPercival, M. David, та Stephen G. Withers. "Applications of enzymes in the synthesis and hydrolytic study of 2-deoxy-α-D-glucopyranosyl phosphate". Canadian Journal of Chemistry 66, № 8 (1 серпня 1988): 1970–72. http://dx.doi.org/10.1139/v88-317.
Повний текст джерелаRajaratnam, Premraj, Praveer Gupta, Peter Katavic, Krystle Kuipers, Ngoc Huyh, Sarah Ryan, Tania Falzun, et al. "Orthogonally Protected Monosaccharide Building Blocks for Solid Phase Production of Diversity Oriented Libraries." Australian Journal of Chemistry 63, no. 4 (2010): 693. http://dx.doi.org/10.1071/ch09480.
Повний текст джерелаDey, Supriya, and Narayanaswamy Jayaraman. "Branching out at C-2 of septanosides. Synthesis of 2-deoxy-2-C-alkyl/aryl septanosides from a bromo-oxepine." Beilstein Journal of Organic Chemistry 8 (April 10, 2012): 522–27. http://dx.doi.org/10.3762/bjoc.8.59.
Повний текст джерелаSchwartz, David A., Ho-Huat Lee, Jeremy P. Carver, and Jiri J. Krepinsky. "Syntheses of model oligosaccharides of biological significance. 4. Synthesis of a fucosylated N,N′-diacetylchitobioside and related oligosaccharides." Canadian Journal of Chemistry 63, no. 5 (May 1, 1985): 1073–79. http://dx.doi.org/10.1139/v85-182.
Повний текст джерелаBest, WM, RW Dunlop, RV Stick та ST White. "All About 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucosyl Trichloroacetimidate". Australian Journal of Chemistry 47, № 3 (1994): 433. http://dx.doi.org/10.1071/ch9940433.
Повний текст джерелаAmbrosio, Gabriella, Tasha Yuliandra, Bernhard Wuest, Monica Mazzarino, Xavier de la Torre, Francesco Botrè, Patrick Diel, Eduard Isenmann, and Maria Kristina Parr. "Urinary Elimination of Ecdysterone and Its Metabolites Following a Single-Dose Administration in Humans." Metabolites 11, no. 6 (June 9, 2021): 366. http://dx.doi.org/10.3390/metabo11060366.
Повний текст джерелаOtero, Iran, Holger Feist, Lidcay Herrera, Manfred Michalik, José Quincoces, and Klaus Peseke. "Nucleoside Analogues from Branched-Chain Pyranosides." Australian Journal of Chemistry 58, no. 2 (2005): 104. http://dx.doi.org/10.1071/ch04168.
Повний текст джерелаLemieux, Raymond U., Rémy Cromer та Ulrike Spohr. "Molecular recognition. VIII. The binding of the β-D-galactopyranosyl residue of the Lewis b human blood group determinant by the lectin IV of Griffonia simplicifolia and by a monoclonal anti-Lewis b antibody. Evidence for intramolecular hydrogen bonding". Canadian Journal of Chemistry 66, № 12 (1 грудня 1988): 3083–98. http://dx.doi.org/10.1139/v88-477.
Повний текст джерелаSun, Zhi Dong, Zi Wen Gong, Chen Hu, Hai Yang Huang, Xi Chen та Qiang Xiao. "Synthesis of an Isomeric Nucleoside Enantiomers of 1,3-bis(1'-deoxy-β-ribofuranose-2'-yl)-thymine". Advanced Materials Research 1094 (березень 2015): 49–52. http://dx.doi.org/10.4028/www.scientific.net/amr.1094.49.
Повний текст джерелаAdachi, K., J. Pang, P. Konitzer, and S. Surrey. "Polymerization of recombinant hemoglobin F gamma E6V and hemoglobin F gamma E6V, gamma Q87T alone, and in mixtures with hemoglobin S." Blood 87, no. 4 (February 15, 1996): 1617–24. http://dx.doi.org/10.1182/blood.v87.4.1617.bloodjournal8741617.
Повний текст джерелаSchwarz, Thomas, David Heß, and Peter Klüfers. "Metal chelation by the common 2-amino-2-deoxy-, 2-N-acetylamino-2-deoxy-, and 2-deoxy-hexoses." Dalton Transactions 39, no. 23 (2010): 5544. http://dx.doi.org/10.1039/c002711a.
Повний текст джерелаPetrakova, Eva, Ulrike Spohr, and Raymond U. Lemieux. "Molecular recognition IX. The synthesis of the H-type 2 human blood group determinant and congeners modified at the 6-position of the N-acetylglucosamine unit." Canadian Journal of Chemistry 70, no. 1 (January 1, 1992): 233–40. http://dx.doi.org/10.1139/v92-034.
Повний текст джерелаNakanishi, H., K. Oguri, K. Yoshida, N. Itano, K. Takenaga, T. Kazama, A. Yoshida, and M. Okayama. "Structural differences between heparan sulphates of proteoglycan involved in the formation of basement membranes in vivo by Lewis-lung-carcinoma-derived cloned cells with different metastatic potentials." Biochemical Journal 288, no. 1 (November 15, 1992): 215–24. http://dx.doi.org/10.1042/bj2880215.
Повний текст джерелаDrašar, Pavel, and Jiří Beránek. "2',3'-O-Carbonyl derivatives of 6-azauridine in the synthesis of its 5-substituted and 5'-deoxy derivatives." Collection of Czechoslovak Chemical Communications 52, no. 8 (1987): 2070–82. http://dx.doi.org/10.1135/cccc19872070.
Повний текст джерелаKollatos, Nikolaos, Christos Mitsos, Stella Manta, Niki Tzioumaki, Christos Giannakas, Tania Alexouli, Aggeliki Panagiotopoulou, Dominique Schols, Graciela Andrei, and Dimitri Komiotis. "Design, Synthesis, and Biological Evaluation of Novel C5-Modified Pyrimidine Ribofuranonucleosides as Potential Antitumor or/and Antiviral Agents." Medicinal Chemistry 16, no. 3 (April 17, 2020): 368–84. http://dx.doi.org/10.2174/1573406415666190225112950.
Повний текст джерелаRoche, Camille J., Tatiana C. Balazs, Qiuying Chen, Juan C. Moreira, Joel M. Friedman та Rhoda Elison Hirsch. "Hemoglobin E (β26Glu→Lys) Exhibits Altered Nitrite Reactivity." Blood 114, № 22 (20 листопада 2009): 2564. http://dx.doi.org/10.1182/blood.v114.22.2564.2564.
Повний текст джерелаMarcotte, Stéphane, Baudoin Gérard, Xavier Pannecoucke, Christian Feasson, and Jean-Charles Quirion. "Synthesis of 3′-Deoxy-3′-difluoromethyluridine and 2′-Deoxy-2′-difluoromethyluridine." Synthesis 2001, no. 06 (2001): 0929–33. http://dx.doi.org/10.1055/s-2001-13419.
Повний текст джерелаGuaragna, Annalisa, Daniele D’Alonzo, Concetta Paolella, and Giovanni Palumbo. "Synthesis of 1-deoxy-l-gulonojirimycin and 1-deoxy-l-talonojirimycin." Tetrahedron Letters 50, no. 18 (May 2009): 2045–47. http://dx.doi.org/10.1016/j.tetlet.2009.02.111.
Повний текст джерелаAamlid, Kai H., Leslie Hough, and Anthony C. Richardson. "Synthesis of 1-deoxy-6-epicastanospermine and 1-deoxy-6,8a-diepicastanospermine." Carbohydrate Research 202 (July 1990): 117–29. http://dx.doi.org/10.1016/0008-6215(90)84075-6.
Повний текст джерелаZhang, Wenhui, Bruce C. Noll та Anthony S. Serianni. "3-Deoxy-β-D-ribo-hexopyranose (3-deoxy-β-D-glucopyranose)". Acta Crystallographica Section C Crystal Structure Communications 63, № 10 (1 вересня 2007): o578—o581. http://dx.doi.org/10.1107/s0108270107038553.
Повний текст джерелаLedvina, Miroslav, David Šaman та Jan Ježek. "Synthesis of O-(2-Deoxy-2-stearoylamino-β-D-glucopyranosyl)-(1→4)-N-acetylnormuramoyl-L-α-aminobutanoyl-D-isoglutamine, a Lipophilic Disaccharide Analogue of MDP". Collection of Czechoslovak Chemical Communications 57, № 3 (1992): 579–89. http://dx.doi.org/10.1135/cccc19920579.
Повний текст джерелаBass, L., W. Bodsch, P. J. Robinson, and M. O. Young. "Metabolites of 2-deoxyglucose in rat brain at 12-24 h: bounds on kinetic constants." American Journal of Physiology-Endocrinology and Metabolism 253, no. 4 (October 1, 1987): E453—E460. http://dx.doi.org/10.1152/ajpendo.1987.253.4.e453.
Повний текст джерелаNagel, Yvonne, and Wolfgang Beck. "Metallkomplexe mit biologisch wichtigen Liganden, XLIII Metallkomplexe mit ungeschützten acyclischen Monosaccharid-Derivaten (Amin-, Oxim-, Schiffbase-, Thiazolidin-und 1,3-Dithian-Liganden)/Metal Complexes with Biologically Important Ligands, XLIII Metal Complexes with Unprotected Acyclic Derivatives of Monosaccharides (Amine, Oxime, Schiffbase, Thiazolidine and 1,3-Dithiane Ligands)." Zeitschrift für Naturforschung B 41, no. 11 (November 1, 1986): 1447–54. http://dx.doi.org/10.1515/znb-1986-1121.
Повний текст джерелаDurham, Timothy B., та William R. Roush. "Stereoselective Synthesis of 2-Deoxy-β-Galactosides via 2-Deoxy-2-bromo- and 2-Deoxy-2-iodo-galactopyranosyl Donors". Organic Letters 5, № 11 (травень 2003): 1871–74. http://dx.doi.org/10.1021/ol034393t.
Повний текст джерелаRobinson, Jared, Indrajit Banerjee, and Alexandra Leclézio. "2-Deoxy D-Glucose in COVID-19: Current Research Trends." Journal of College of Medical Sciences-Nepal 18, no. 1 (March 31, 2022): 80–84. http://dx.doi.org/10.3126/jcmsn.v18i1.37651.
Повний текст джерелаOffer, J., J. C. Metcalfe, and G. A. Smith. "The uptake of 3H-labelled monodeoxyfluoro-myo-inositols into thymocytes and their incorporation into phospholipid in permeabilized cells." Biochemical Journal 291, no. 2 (April 15, 1993): 553–60. http://dx.doi.org/10.1042/bj2910553.
Повний текст джерелаKefurt, Karel, Karel Čapek, Zdeňka Kefurtová, and Jiří Jarý. "Preparation of 6-amino-6-deoxy-D-altronic acid and their derivatives." Collection of Czechoslovak Chemical Communications 51, no. 2 (1986): 391–400. http://dx.doi.org/10.1135/cccc19860391.
Повний текст джерелаHanessian, Stephen, Oscar M. Saavedra, Miguel A. Vilchis-Reyes, and Ana M. Llaguno-Rueda. "Synthesis of 4′-deoxy-4′-fluoro neamine and 4′-deoxy-4′-fluoro 4′-epi neamine." MedChemComm 5, no. 8 (2014): 1166–71. http://dx.doi.org/10.1039/c4md00072b.
Повний текст джерелаLee, Jin W., Fang Deng, Walter G. Yeomans, Alfred L. Allen, Richard A. Gross, and David L. Kaplan. "Direct Incorporation of Glucosamine andN-Acetylglucosamine into Exopolymers byGluconacetobacter xylinus (=Acetobacter xylinum) ATCC 10245: Production of Chitosan-Cellulose and Chitin-Cellulose Exopolymers." Applied and Environmental Microbiology 67, no. 9 (September 1, 2001): 3970–75. http://dx.doi.org/10.1128/aem.67.9.3970-3975.2001.
Повний текст джерелаBird, P., D. H. Dolphin, and S. G. Withers. "The synthesis of protected 5-azido-5-deoxy-D-glucononitriles as precursors of glycosidase inhibitors." Canadian Journal of Chemistry 68, no. 2 (February 1, 1990): 317–22. http://dx.doi.org/10.1139/v90-045.
Повний текст джерелаLin, Zhen-Jian, Tian-Jiao Zhu, Guo-Jian Zhang, Hong-Juan Wei, and Qian-Qun Gu. "Deoxy-cytochalasins from a marine-derived fungus Spicaria elegans." Canadian Journal of Chemistry 87, no. 3 (March 2009): 486–89. http://dx.doi.org/10.1139/v09-006.
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