Статті в журналах з теми "Dideoxy sugars"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Dideoxy sugars".
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Driguez, H., JC Mcauliffe, RV Stick, DMG Tilbrook, and SJ Williams. "A New Approach to Some 1,6-Dideoxy 1,6-Epithio Sugars." Australian Journal of Chemistry 49, no. 3 (1996): 343. http://dx.doi.org/10.1071/ch9960343.
Повний текст джерелаFatima, Ayjaz, Abdul Malik, and Wolfgang Voelter. "A Novel Entry into Cyclopropanated Sugar Amino Acids." Zeitschrift für Naturforschung B 49, no. 10 (October 1, 1994): 1434–38. http://dx.doi.org/10.1515/znb-1994-1021.
Повний текст джерелаConway, RJ, JP Nagel, RV Stick, and DMG Tilbrook. "Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride." Australian Journal of Chemistry 38, no. 6 (1985): 939. http://dx.doi.org/10.1071/ch9850939.
Повний текст джерелаShishmarev, Dmitry, Lucas Quiquempoix, Clément Q. Fontenelle, Bruno Linclau, and Philip W. Kuchel. "Anomerisation of Fluorinated Sugars by Mutarotase Studied Using 19F NMR Two-Dimensional Exchange Spectroscopy." Australian Journal of Chemistry 73, no. 3 (2020): 117. http://dx.doi.org/10.1071/ch19562.
Повний текст джерелаBinkley, Roger W., and Mahmoud A. Abdulaziz. "Synthesis of dideoxy sugars by triflate rearrangement." Journal of Organic Chemistry 52, no. 21 (October 1987): 4713–17. http://dx.doi.org/10.1021/jo00230a011.
Повний текст джерелаZhang, Guisheng, Lei Shi, Qingfeng Liu, Jingmei Wang, Lu Li, and Xiaobing Liu. "A divergent strategy for constructing a sugar library containing 2,6-dideoxy sugars and uncommon sugars with 4-substitution." Tetrahedron 63, no. 39 (September 2007): 9705–11. http://dx.doi.org/10.1016/j.tet.2007.07.019.
Повний текст джерелаSiu, Sarah, Anna Robotham, Susan M. Logan, John F. Kelly, Kaoru Uchida, Shin-Ichi Aizawa, and 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, no. 9 (March 2, 2015): 1668–80. http://dx.doi.org/10.1128/jb.00040-15.
Повний текст джерелаWang, Ying, Yanli Xu, Andrei V. Perepelov, Yuanyuan Qi, Yuriy A. Knirel, Lei Wang, and 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, no. 23 (September 28, 2007): 8626–35. http://dx.doi.org/10.1128/jb.00777-07.
Повний текст джерелаLiu, Song Yu, and John P. N. Rosazza. "Enzymatic Conversion of Glucose to UDP-4-Keto-6-Deoxyglucose in Streptomyces spp." Applied and Environmental Microbiology 64, no. 10 (October 1, 1998): 3972–76. http://dx.doi.org/10.1128/aem.64.10.3972-3976.1998.
Повний текст джерелаToshima, Kazunobu, Takehito Yoshida, Satsuki Mukaiyama, and Kuniaki Tatsuta. "De novo highly stereocontrolled synthesis of 2,6-dideoxy sugars by use of 2,6-anhydro-2-thio sugars." Carbohydrate Research 222 (December 1991): 173–88. http://dx.doi.org/10.1016/0008-6215(91)89016-9.
Повний текст джерелаMiljkovic, Momcilo, and Margaret Habash-Marino. "Synthesis of higher sugars as precursors for the synthesis of chiral polyhydroxylated macrocyclic lactones." Journal of the Serbian Chemical Society 65, no. 7 (2000): 497–505. http://dx.doi.org/10.2298/jsc0007497m.
Повний текст джерелаHung, Ming-Ni, Erumbi Rangarajan, Christine Munger, Guy Nadeau, Traian Sulea, and Allan Matte. "Crystal Structure of TDP-Fucosamine Acetyltransferase (WecD) from Escherichia coli, an Enzyme Required for Enterobacterial Common Antigen Synthesis." Journal of Bacteriology 188, no. 15 (August 1, 2006): 5606–17. http://dx.doi.org/10.1128/jb.00306-06.
Повний текст джерелаDemendi, Melinda, and Carole Creuzenet. "Cj1123c (PglD), a multifaceted acetyltransferase from Campylobacter jejuni." Biochemistry and Cell Biology 87, no. 3 (June 2009): 469–83. http://dx.doi.org/10.1139/o09-002.
Повний текст джерелаColeman, Robert S., and Janet R. Fraser. "Acylketene [4+2] cycloadditions: divergent de novo synthesis of 2,6-dideoxy sugars." Journal of Organic Chemistry 58, no. 2 (January 1993): 385–92. http://dx.doi.org/10.1021/jo00054a022.
Повний текст джерелаDRIGUEZ, H., J. C. MCAULIFFE, R. V. STICK, D. M. G. TILBROOK, and S. J. WILLIAMS. "ChemInform Abstract: A New Approach to Some 1,6-Dideoxy 1,6-Epithio Sugars." ChemInform 27, no. 35 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199635212.
Повний текст джерелаal Daher, S., G. Fleet, S. K. Namgoong, and B. Winchester. "Change in specificity of glycosidase inhibition by N-alkylation of amino sugars." Biochemical Journal 258, no. 2 (March 1, 1989): 613–15. http://dx.doi.org/10.1042/bj2580613.
Повний текст джерелаKing, Jerry D., Erin F. Mulrooney, Evgeny Vinogradov, Bernd Kneidinger, Kristen Mead, and 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, no. 5 (December 21, 2007): 1671–79. http://dx.doi.org/10.1128/jb.01708-07.
Повний текст джерелаNogueira, Jason M., Marissa Bylsma, Danielle K. Bright та Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars". Angewandte Chemie International Edition 55, № 34 (19 липня 2016): 10088–92. http://dx.doi.org/10.1002/anie.201605091.
Повний текст джерелаNogueira, Jason M., Marissa Bylsma, Danielle K. Bright та Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars". Angewandte Chemie 128, № 34 (19 липня 2016): 10242–46. http://dx.doi.org/10.1002/ange.201605091.
Повний текст джерелаShekhani, Mohammed Saleh, Farzane Latif, Ayjaz Fatima, Abdul Malik, and 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, no. 21 (1988): 1419. http://dx.doi.org/10.1039/c39880001419.
Повний текст джерелаDing, Feiqing, Shuting Cai, Ronny William, and Xue-Wei Liu. "Pathways leading to 3-amino- and 3-nitro-2,3-dideoxy sugars: strategies and synthesis." RSC Advances 3, no. 33 (2013): 13594. http://dx.doi.org/10.1039/c3ra40595h.
Повний текст джерелаSchmidt, Richard R., and Martin Maier. "Diastereospecific synthesis of 2.6-dideoxy- and 2.4.6-trideoxy-sugars via hetero-diels-alder-reaction." Tetrahedron Letters 26, no. 17 (1985): 2065–68. http://dx.doi.org/10.1016/s0040-4039(00)94780-4.
Повний текст джерелаBinkley, Roger W. "Inversion of configuration in 2,6-dideoxy sugars. Triflate displacement by benzoate and nitrite anions." Journal of Organic Chemistry 56, no. 12 (June 1991): 3892–96. http://dx.doi.org/10.1021/jo00012a020.
Повний текст джерелаCOLEMAN, R. S., and J. R. FRASER. "ChemInform Abstract: Acylketene (4 + 2)Cycloadditions: Divergent de Novo Synthesis of 2,6- Dideoxy Sugars." ChemInform 24, no. 21 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199321227.
Повний текст джерелаTOSHIMA, Kazunobu, and 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, no. 4 (1992): 303–15. http://dx.doi.org/10.5059/yukigoseikyokaishi.50.303.
Повний текст джерелаIshii, Nozomi. "α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars Using Cyclic Geminal Dihalides". Trends in Glycoscience and Glycotechnology 34, № 199 (27 травня 2022): E61. http://dx.doi.org/10.4052/tigg.2205.6e.
Повний текст джерелаIshii, Nozomi. "α-Selective Dehydrative Glycosylation of 2-Deoxy- and 2,6-Dideoxy Sugars Using Cyclic Geminal Dihalides". Trends in Glycoscience and Glycotechnology 34, № 199 (27 травня 2022): J61. http://dx.doi.org/10.4052/tigg.2205.6j.
Повний текст джерелаPieper, Patricia A., Zhihong Guo, and 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, no. 18 (May 1995): 5158–59. http://dx.doi.org/10.1021/ja00123a021.
Повний текст джерелаDancy, Isabelle, Lothar Laupichler, Patrick Rollin, and Joachim Thiem. "Efficient Synthesis of Deoxy and Dideoxy Sugars by a Thio-Mitsunobu Reaction on Unprotected Glycosides." Synlett 1992, no. 04 (1992): 283–84. http://dx.doi.org/10.1055/s-1992-21340.
Повний текст джерелаRomeo, Joseph R., Luca McDermott та Clay S. Bennett. "Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy Sugars: Construction of the Arugomycin Tetrasaccharide". Organic Letters 22, № 9 (13 квітня 2020): 3649–54. http://dx.doi.org/10.1021/acs.orglett.0c01153.
Повний текст джерелаBerrocal, M. V., M. V. Gil, E. Román, J. A. Serrano, M. B. Hursthouse, and M. E. Light. "Tandem Michael addition and intramolecular aldol cyclization of 1,2-dideoxy-1-nitroheptitols derived from sugars." Tetrahedron Letters 46, no. 21 (May 2005): 3673–76. http://dx.doi.org/10.1016/j.tetlet.2005.03.162.
Повний текст джерелаWinchester, B., C. Barker, S. Baines, G. S. Jacob, S. K. Namgoong та G. Fleet. "Inhibition of α-l-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin". Biochemical Journal 265, № 1 (1 січня 1990): 277–82. http://dx.doi.org/10.1042/bj2650277.
Повний текст джерелаJaved, Ashwani Tiwari, Zanjila Azeem та 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, № 5 (21 січня 2022): 3718–29. http://dx.doi.org/10.1021/acs.joc.1c02650.
Повний текст джерелаBinkley, Roger W., Edith R. Binkley, Shaoming Duan, Michael J. S. Tevesz, and Witold Winnik. "Negative-Ion Mass Spectrometry of Carbohydrates. A Mechanistic Study of the Fragmentation Reactions of Dideoxy Sugars." Journal of Carbohydrate Chemistry 15, no. 7 (September 1996): 879–95. http://dx.doi.org/10.1080/07328309608005697.
Повний текст джерелаBINKLEY, R. W. "ChemInform Abstract: Inversion of Configuration in 2,6-Dideoxy Sugars. Triflate Displacement by Benzoate and Nitrite Anions." ChemInform 22, no. 44 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199144279.
Повний текст джерелаDing, Feiqing, Shuting Cai, Ronny William, and Xue-Wei Liu. "ChemInform Abstract: Pathways Leading to 3-Amino- and 3-Nitro-2,3-dideoxy Sugars: Strategies and Synthesis." ChemInform 44, no. 41 (September 19, 2013): no. http://dx.doi.org/10.1002/chin.201341241.
Повний текст джерелаHerak, Janko N., та 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, № 11-12 (1 грудня 1986): 1062–68. http://dx.doi.org/10.1515/znc-1986-11-1219.
Повний текст джерелаTurek, Dominika, Andreas Sundgren, Martina Lahmann, and Stefan Oscarson. "Synthesis of oligosaccharides corresponding to Vibrio cholerae O139 polysaccharide structures containing dideoxy sugars and a cyclic phosphate." Organic & Biomolecular Chemistry 4, no. 7 (2006): 1236. http://dx.doi.org/10.1039/b518125a.
Повний текст джерелаYamazaki, Takashi, Kenji Mizutani, and 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, no. 19 (September 1995): 6046–56. http://dx.doi.org/10.1021/jo00124a013.
Повний текст джерелаTronchet, Jean M. J., Nicoletta Bizzozero, Martina Zsély, Françoise Barbalat-Rey, Naz Dolatshahi, Gerald Bernardinelli та Michel Geoffroy. "Deoxyhydroxyamino analogs of sugars: derivatives of methyl 2,3-dideoxy-2-hydroxyamino-α-d-arabino- and -lyxo-hexopyranosides". Carbohydrate Research 212 (червень 1991): 65–76. http://dx.doi.org/10.1016/0008-6215(91)84046-h.
Повний текст джерелаMizutani, Kenji, Takashi Yamazaki, and 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, no. 1 (1995): 51. http://dx.doi.org/10.1039/c39950000051.
Повний текст джерелаDANCY, I., L. LAUPICHLER, P. ROLLIN, and J. THIEM. "ChemInform Abstract: Efficient Synthesis of Deoxy and Dideoxy Sugars by a Thio-Mitsunobu Reaction on Unprotected Glycosides." ChemInform 23, no. 39 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199239285.
Повний текст джерелаTOSHIMA, K., and K. TATSUTA. "ChemInform Abstract: Highly Stereocontrolled Synthesis of 2,6-Dideoxy Sugars and Its Application to Synthesis of Natural Products." ChemInform 23, no. 47 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199247309.
Повний текст джерелаHaque, Md Ekuramul, Tohoru Kikuchi, Kimihiro Kanemitsu, and Yoshisuke Tsuda. "Synthesis of some deoxy, unsaturated, and dideoxy sugars via regioselective thioacylation of glycopyranosides by the dibutyltin oxide method." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 1 (1986): 430–33. http://dx.doi.org/10.1248/cpb.34.430.
Повний текст джерелаCao, Ji, Masazumi Tamura, Ryu Hosaka, Akira Nakayama, Jun-ya Hasegawa, Yoshinao Nakagawa, and Keiichi Tomishige. "Mechanistic Study on Deoxydehydration and Hydrogenation of Methyl Glycosides to Dideoxy Sugars over a ReOx–Pd/CeO2 Catalyst." ACS Catalysis 10, no. 20 (September 16, 2020): 12040–51. http://dx.doi.org/10.1021/acscatal.0c02309.
Повний текст джерелаToshima, Kazunobu, Satsuki Mukaiyama, Yuko Nozaki, Hatsuki Inokuchi, Masaya Nakata, and 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, no. 20 (October 1994): 9042–51. http://dx.doi.org/10.1021/ja00099a022.
Повний текст джерелаMIZUTANI, K., T. YAMAZAKI, and 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, no. 23 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199523210.
Повний текст джерелаKajimura, Junko, Arifur Rahman, James Hsu, Matthew R. Evans, Kevin H. Gardner, and 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, no. 21 (August 25, 2006): 7542–50. http://dx.doi.org/10.1128/jb.00783-06.
Повний текст джерелаKolar, Cenek, Konrad Dehmel та 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 (грудень 1990): 67–81. http://dx.doi.org/10.1016/0008-6215(90)80086-i.
Повний текст джерелаGelas-Mialhe, Yvonne, та 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, № 2 (червень 1990): 243–47. http://dx.doi.org/10.1016/0008-6215(90)84267-x.
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