Artículos de revistas sobre el tema "Dideoxy sugars"
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Driguez, H., JC Mcauliffe, RV Stick, DMG Tilbrook y SJ Williams. "A New Approach to Some 1,6-Dideoxy 1,6-Epithio Sugars". Australian Journal of Chemistry 49, n.º 3 (1996): 343. http://dx.doi.org/10.1071/ch9960343.
Texto completoFatima, Ayjaz, Abdul Malik y Wolfgang Voelter. "A Novel Entry into Cyclopropanated Sugar Amino Acids". Zeitschrift für Naturforschung B 49, n.º 10 (1 de octubre de 1994): 1434–38. http://dx.doi.org/10.1515/znb-1994-1021.
Texto completoConway, RJ, JP Nagel, RV Stick y DMG Tilbrook. "Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride". Australian Journal of Chemistry 38, n.º 6 (1985): 939. http://dx.doi.org/10.1071/ch9850939.
Texto completoShishmarev, Dmitry, Lucas Quiquempoix, Clément Q. Fontenelle, Bruno Linclau y Philip W. Kuchel. "Anomerisation of Fluorinated Sugars by Mutarotase Studied Using 19F NMR Two-Dimensional Exchange Spectroscopy". Australian Journal of Chemistry 73, n.º 3 (2020): 117. http://dx.doi.org/10.1071/ch19562.
Texto completoBinkley, Roger W. y Mahmoud A. Abdulaziz. "Synthesis of dideoxy sugars by triflate rearrangement". Journal of Organic Chemistry 52, n.º 21 (octubre de 1987): 4713–17. http://dx.doi.org/10.1021/jo00230a011.
Texto completoZhang, Guisheng, Lei Shi, Qingfeng Liu, Jingmei Wang, Lu Li y Xiaobing Liu. "A divergent strategy for constructing a sugar library containing 2,6-dideoxy sugars and uncommon sugars with 4-substitution". Tetrahedron 63, n.º 39 (septiembre de 2007): 9705–11. http://dx.doi.org/10.1016/j.tet.2007.07.019.
Texto completoSiu, Sarah, Anna Robotham, Susan M. Logan, John F. Kelly, Kaoru Uchida, Shin-Ichi Aizawa y Ken F. Jarrell. "Evidence that Biosynthesis of the Second and Third Sugars of the Archaellin Tetrasaccharide in the Archaeon Methanococcus maripaludis Occurs by the Same Pathway Used by Pseudomonas aeruginosa To Make a Di-N-Acetylated Sugar". Journal of Bacteriology 197, n.º 9 (2 de marzo de 2015): 1668–80. http://dx.doi.org/10.1128/jb.00040-15.
Texto completoWang, Ying, Yanli Xu, Andrei V. Perepelov, Yuanyuan Qi, Yuriy A. Knirel, Lei Wang y Lu Feng. "Biochemical Characterization of dTDP-d-Qui4N and dTDP-d-Qui4NAc Biosynthetic Pathways in Shigella dysenteriae Type 7 and Escherichia coli O7". Journal of Bacteriology 189, n.º 23 (28 de septiembre de 2007): 8626–35. http://dx.doi.org/10.1128/jb.00777-07.
Texto completoLiu, Song Yu y John P. N. Rosazza. "Enzymatic Conversion of Glucose to UDP-4-Keto-6-Deoxyglucose in Streptomyces spp". Applied and Environmental Microbiology 64, n.º 10 (1 de octubre de 1998): 3972–76. http://dx.doi.org/10.1128/aem.64.10.3972-3976.1998.
Texto completoToshima, Kazunobu, Takehito Yoshida, Satsuki Mukaiyama y Kuniaki Tatsuta. "De novo highly stereocontrolled synthesis of 2,6-dideoxy sugars by use of 2,6-anhydro-2-thio sugars". Carbohydrate Research 222 (diciembre de 1991): 173–88. http://dx.doi.org/10.1016/0008-6215(91)89016-9.
Texto completoMiljkovic, Momcilo y Margaret Habash-Marino. "Synthesis of higher sugars as precursors for the synthesis of chiral polyhydroxylated macrocyclic lactones". Journal of the Serbian Chemical Society 65, n.º 7 (2000): 497–505. http://dx.doi.org/10.2298/jsc0007497m.
Texto completoHung, Ming-Ni, Erumbi Rangarajan, Christine Munger, Guy Nadeau, Traian Sulea y Allan Matte. "Crystal Structure of TDP-Fucosamine Acetyltransferase (WecD) from Escherichia coli, an Enzyme Required for Enterobacterial Common Antigen Synthesis". Journal of Bacteriology 188, n.º 15 (1 de agosto de 2006): 5606–17. http://dx.doi.org/10.1128/jb.00306-06.
Texto completoDemendi, Melinda y Carole Creuzenet. "Cj1123c (PglD), a multifaceted acetyltransferase from Campylobacter jejuni". Biochemistry and Cell Biology 87, n.º 3 (junio de 2009): 469–83. http://dx.doi.org/10.1139/o09-002.
Texto completoColeman, Robert S. y Janet R. Fraser. "Acylketene [4+2] cycloadditions: divergent de novo synthesis of 2,6-dideoxy sugars". Journal of Organic Chemistry 58, n.º 2 (enero de 1993): 385–92. http://dx.doi.org/10.1021/jo00054a022.
Texto completoDRIGUEZ, H., J. C. MCAULIFFE, R. V. STICK, D. M. G. TILBROOK y S. J. WILLIAMS. "ChemInform Abstract: A New Approach to Some 1,6-Dideoxy 1,6-Epithio Sugars." ChemInform 27, n.º 35 (5 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199635212.
Texto completoal Daher, S., G. Fleet, S. K. Namgoong y B. Winchester. "Change in specificity of glycosidase inhibition by N-alkylation of amino sugars". Biochemical Journal 258, n.º 2 (1 de marzo de 1989): 613–15. http://dx.doi.org/10.1042/bj2580613.
Texto completoKing, Jerry D., Erin F. Mulrooney, Evgeny Vinogradov, Bernd Kneidinger, Kristen Mead y Joseph S. Lam. "lfnA from Pseudomonas aeruginosa O12 and wbuX from Escherichia coli O145 Encode Membrane-Associated Proteins and Are Required for Expression of 2,6-Dideoxy-2-Acetamidino-l-Galactose in Lipopolysaccharide O Antigen". Journal of Bacteriology 190, n.º 5 (21 de diciembre de 2007): 1671–79. http://dx.doi.org/10.1128/jb.01708-07.
Texto completoNogueira, Jason M., Marissa Bylsma, Danielle K. Bright y Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars". Angewandte Chemie International Edition 55, n.º 34 (19 de julio de 2016): 10088–92. http://dx.doi.org/10.1002/anie.201605091.
Texto completoNogueira, Jason M., Marissa Bylsma, Danielle K. Bright y Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars". Angewandte Chemie 128, n.º 34 (19 de julio de 2016): 10242–46. http://dx.doi.org/10.1002/ange.201605091.
Texto completoShekhani, Mohammed Saleh, Farzane Latif, Ayjaz Fatima, Abdul Malik y Wolfgang Voelter. "Synthesis of 3,4-dideoxy-3,4-C-cyanomethylene pyranosides: a new class of cyclopropanated sugars". Journal of the Chemical Society, Chemical Communications, n.º 21 (1988): 1419. http://dx.doi.org/10.1039/c39880001419.
Texto completoDing, Feiqing, Shuting Cai, Ronny William y Xue-Wei Liu. "Pathways leading to 3-amino- and 3-nitro-2,3-dideoxy sugars: strategies and synthesis". RSC Advances 3, n.º 33 (2013): 13594. http://dx.doi.org/10.1039/c3ra40595h.
Texto completoSchmidt, Richard R. y Martin Maier. "Diastereospecific synthesis of 2.6-dideoxy- and 2.4.6-trideoxy-sugars via hetero-diels-alder-reaction". Tetrahedron Letters 26, n.º 17 (1985): 2065–68. http://dx.doi.org/10.1016/s0040-4039(00)94780-4.
Texto completoBinkley, Roger W. "Inversion of configuration in 2,6-dideoxy sugars. Triflate displacement by benzoate and nitrite anions". Journal of Organic Chemistry 56, n.º 12 (junio de 1991): 3892–96. http://dx.doi.org/10.1021/jo00012a020.
Texto completoCOLEMAN, R. S. y J. R. FRASER. "ChemInform Abstract: Acylketene (4 + 2)Cycloadditions: Divergent de Novo Synthesis of 2,6- Dideoxy Sugars." ChemInform 24, n.º 21 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199321227.
Texto completoTOSHIMA, Kazunobu y Kuniaki TATSUTA. "Highly Stereocontrolled Synthesis of 2,6-Dideoxy Sugars and Its Application to Synthesis of Natural Products." Journal of Synthetic Organic Chemistry, Japan 50, n.º 4 (1992): 303–15. http://dx.doi.org/10.5059/yukigoseikyokaishi.50.303.
Texto completoIshii, Nozomi. "α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars Using Cyclic Geminal Dihalides". Trends in Glycoscience and Glycotechnology 34, n.º 199 (27 de mayo de 2022): E61. http://dx.doi.org/10.4052/tigg.2205.6e.
Texto completoIshii, Nozomi. "α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars Using Cyclic Geminal Dihalides". Trends in Glycoscience and Glycotechnology 34, n.º 199 (27 de mayo de 2022): J61. http://dx.doi.org/10.4052/tigg.2205.6j.
Texto completoPieper, Patricia A., Zhihong Guo y Hung-wen Liu. "Mechanistic Studies of the Biosynthesis of 3,6-Dideoxy Sugars: Stereochemical Analysis of C-3 Deoxygenation". Journal of the American Chemical Society 117, n.º 18 (mayo de 1995): 5158–59. http://dx.doi.org/10.1021/ja00123a021.
Texto completoDancy, Isabelle, Lothar Laupichler, Patrick Rollin y Joachim Thiem. "Efficient Synthesis of Deoxy and Dideoxy Sugars by a Thio-Mitsunobu Reaction on Unprotected Glycosides". Synlett 1992, n.º 04 (1992): 283–84. http://dx.doi.org/10.1055/s-1992-21340.
Texto completoRomeo, Joseph R., Luca McDermott y Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy Sugars: Construction of the Arugomycin Tetrasaccharide". Organic Letters 22, n.º 9 (13 de abril de 2020): 3649–54. http://dx.doi.org/10.1021/acs.orglett.0c01153.
Texto completoBerrocal, M. V., M. V. Gil, E. Román, J. A. Serrano, M. B. Hursthouse y M. E. Light. "Tandem Michael addition and intramolecular aldol cyclization of 1,2-dideoxy-1-nitroheptitols derived from sugars". Tetrahedron Letters 46, n.º 21 (mayo de 2005): 3673–76. http://dx.doi.org/10.1016/j.tetlet.2005.03.162.
Texto completoWinchester, B., C. Barker, S. Baines, G. S. Jacob, S. K. Namgoong y G. Fleet. "Inhibition of α-l-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin". Biochemical Journal 265, n.º 1 (1 de enero de 1990): 277–82. http://dx.doi.org/10.1042/bj2650277.
Texto completoJaved, Ashwani Tiwari, Zanjila Azeem y Pintu Kumar Mandal. "4,5-Dioxo-imidazolinium Cation-Promoted α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars". Journal of Organic Chemistry 87, n.º 5 (21 de enero de 2022): 3718–29. http://dx.doi.org/10.1021/acs.joc.1c02650.
Texto completoBinkley, Roger W., Edith R. Binkley, Shaoming Duan, Michael J. S. Tevesz y Witold Winnik. "Negative-Ion Mass Spectrometry of Carbohydrates. A Mechanistic Study of the Fragmentation Reactions of Dideoxy Sugars". Journal of Carbohydrate Chemistry 15, n.º 7 (septiembre de 1996): 879–95. http://dx.doi.org/10.1080/07328309608005697.
Texto completoBINKLEY, R. W. "ChemInform Abstract: Inversion of Configuration in 2,6-Dideoxy Sugars. Triflate Displacement by Benzoate and Nitrite Anions." ChemInform 22, n.º 44 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199144279.
Texto completoDing, Feiqing, Shuting Cai, Ronny William y Xue-Wei Liu. "ChemInform Abstract: Pathways Leading to 3-Amino- and 3-Nitro-2,3-dideoxy Sugars: Strategies and Synthesis". ChemInform 44, n.º 41 (19 de septiembre de 2013): no. http://dx.doi.org/10.1002/chin.201341241.
Texto completoHerak, Janko N. y Günter Behrens. "Formation and Structure of Radicals from ᴅ-Ribose and 2-Deoxy- ᴅ-ribose by Reactions with SO4·̅ Radicals in Aqueous Solution. An in-situ Electron Spin Resonance Study". Zeitschrift für Naturforschung C 41, n.º 11-12 (1 de diciembre de 1986): 1062–68. http://dx.doi.org/10.1515/znc-1986-11-1219.
Texto completoTurek, Dominika, Andreas Sundgren, Martina Lahmann y Stefan Oscarson. "Synthesis of oligosaccharides corresponding to Vibrio cholerae O139 polysaccharide structures containing dideoxy sugars and a cyclic phosphate". Organic & Biomolecular Chemistry 4, n.º 7 (2006): 1236. http://dx.doi.org/10.1039/b518125a.
Texto completoYamazaki, Takashi, Kenji Mizutani y Tomoya Kitazume. "Modified Preparation Method of Trifluoromethylated Propargylic Alcohols and Its Application to Chiral 2,6-Dideoxy-6,6,6-trifluoro sugars". Journal of Organic Chemistry 60, n.º 19 (septiembre de 1995): 6046–56. http://dx.doi.org/10.1021/jo00124a013.
Texto completoTronchet, Jean M. J., Nicoletta Bizzozero, Martina Zsély, Françoise Barbalat-Rey, Naz Dolatshahi, Gerald Bernardinelli y Michel Geoffroy. "Deoxyhydroxyamino analogs of sugars: derivatives of methyl 2,3-dideoxy-2-hydroxyamino-α-d-arabino- and -lyxo-hexopyranosides". Carbohydrate Research 212 (junio de 1991): 65–76. http://dx.doi.org/10.1016/0008-6215(91)84046-h.
Texto completoMizutani, Kenji, Takashi Yamazaki y Tomoya Kitazume. "Novel stereoselective syntheses of chiral 2,6-dideoxy-6,6,6-trifluoro sugars via enzymatic resolution of trifluoromethylated propynylic alcohol". Journal of the Chemical Society, Chemical Communications, n.º 1 (1995): 51. http://dx.doi.org/10.1039/c39950000051.
Texto completoDANCY, I., L. LAUPICHLER, P. ROLLIN y J. THIEM. "ChemInform Abstract: Efficient Synthesis of Deoxy and Dideoxy Sugars by a Thio-Mitsunobu Reaction on Unprotected Glycosides." ChemInform 23, n.º 39 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199239285.
Texto completoTOSHIMA, K. y K. TATSUTA. "ChemInform Abstract: Highly Stereocontrolled Synthesis of 2,6-Dideoxy Sugars and Its Application to Synthesis of Natural Products". ChemInform 23, n.º 47 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199247309.
Texto completoHaque, Md Ekuramul, Tohoru Kikuchi, Kimihiro Kanemitsu y Yoshisuke Tsuda. "Synthesis of some deoxy, unsaturated, and dideoxy sugars via regioselective thioacylation of glycopyranosides by the dibutyltin oxide method." CHEMICAL & PHARMACEUTICAL BULLETIN 34, n.º 1 (1986): 430–33. http://dx.doi.org/10.1248/cpb.34.430.
Texto completoCao, Ji, Masazumi Tamura, Ryu Hosaka, Akira Nakayama, Jun-ya Hasegawa, Yoshinao Nakagawa y Keiichi Tomishige. "Mechanistic Study on Deoxydehydration and Hydrogenation of Methyl Glycosides to Dideoxy Sugars over a ReOx–Pd/CeO2 Catalyst". ACS Catalysis 10, n.º 20 (16 de septiembre de 2020): 12040–51. http://dx.doi.org/10.1021/acscatal.0c02309.
Texto completoToshima, Kazunobu, Satsuki Mukaiyama, Yuko Nozaki, Hatsuki Inokuchi, Masaya Nakata y Kuniaki Tatsuta. "Novel Glycosidation Method Using 2,6-Anhydro-2-thio Sugars for Stereocontrolled Synthesis of 2,6-Dideoxy-.alpha.- and -.beta.-glycosides". Journal of the American Chemical Society 116, n.º 20 (octubre de 1994): 9042–51. http://dx.doi.org/10.1021/ja00099a022.
Texto completoMIZUTANI, K., T. YAMAZAKI y T. KITAZUME. "ChemInform Abstract: Novel Stereoselective Syntheses of Chiral 2,6-Dideoxy-6,6,6-trifluoro Sugars via Enzymatic Resolution of Trifluoromethylated Propynylic Alcohol." ChemInform 26, n.º 23 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199523210.
Texto completoKajimura, Junko, Arifur Rahman, James Hsu, Matthew R. Evans, Kevin H. Gardner y Paul D. Rick. "O Acetylation of the Enterobacterial Common Antigen Polysaccharide Is Catalyzed by the Product of the yiaH Gene of Escherichia coli K-12". Journal of Bacteriology 188, n.º 21 (25 de agosto de 2006): 7542–50. http://dx.doi.org/10.1128/jb.00783-06.
Texto completoKolar, Cenek, Konrad Dehmel y Hans Moldenhauer. "Synthesis of 4-O-methyl-β-rhodomycins using derivatives of 4-amino-4-deoxy- and 3,4-diamino-3,4-dideoxy sugars". Carbohydrate Research 208 (diciembre de 1990): 67–81. http://dx.doi.org/10.1016/0008-6215(90)80086-i.
Texto completoGelas-Mialhe, Yvonne y Jacques Gelas. "New branched-chain and aminodeoxy sugars from 1,6-anhydro-3,4-dideoxy-β-d-glycero-hex-3-enopyranos-2-ulose (levoglucosenone)". Carbohydrate Research 199, n.º 2 (junio de 1990): 243–47. http://dx.doi.org/10.1016/0008-6215(90)84267-x.
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