Literatura académica sobre el tema "Anomeric position"
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Artículos de revistas sobre el tema "Anomeric position"
Filho, João Rufino de Freitas, Jucleiton José Rufino de Freitas, Pedro Ramos de Souza Neto, Fabrícia Aparecida Marques de Souza, Adiel Soares Ferreira, Anne Gabrielle Marques da Silva, Francisco Antonio Mabson Henrique Lopes, Marcilio Martins de Moraes, Clécio Souza Ramos y Ronaldo Nascimentos de Oliveira. "Recent Advances Related to Anomeric and Exo-anomeric Effects in Carbohydrate Chemistry". International Research Journal of Pure and Applied Chemistry 24, n.º 5 (22 de septiembre de 2023): 95–110. http://dx.doi.org/10.9734/irjpac/2023/v24i5830.
Texto completoJabbari, Hadi. "Selective Anomeric Deacetylation of Per-Acetylated Carbohydrates Using (i-Pr)3Sn(OEt) and Synthesis of New Derivatives". Journal of Molecular Biology Research 10, n.º 1 (30 de noviembre de 2020): 166. http://dx.doi.org/10.5539/jmbr.v10n1p166.
Texto completoLee, Sang Jun, Dale E. A. Lewis y Sankar Adhya. "Induction of the Galactose Enzymes in Escherichia coli Is Independent of the C-1-Hydroxyl Optical Configuration of the Inducer d-Galactose". Journal of Bacteriology 190, n.º 24 (17 de octubre de 2008): 7932–38. http://dx.doi.org/10.1128/jb.01008-08.
Texto completoÖlgen, Süreyya y Chung K. Chu. "Synthesis And Antiviral Activity Of 2'-Deoxy-2'-Fluoro-L-Arabinofuranosyl 1,2,3-Triazole Derivatives". Zeitschrift für Naturforschung B 56, n.º 8 (1 de agosto de 2001): 804–11. http://dx.doi.org/10.1515/znb-2001-0814.
Texto completoEstevez, Juan C., Helen Ardron, Mark R. Wormald, David Brown y George W. J. Fleet. "Spirocyclic peptides at the anomeric position of mannofuranose". Tetrahedron Letters 35, n.º 47 (noviembre de 1994): 8889–90. http://dx.doi.org/10.1016/s0040-4039(00)78526-1.
Texto completoTanzi, Lisa, Marina Simona Robescu, Sara Marzatico, Teresa Recca, Yongmin Zhang, Marco Terreni y Teodora Bavaro. "Developing a Library of Mannose-Based Mono- and Disaccharides: A General Chemoenzymatic Approach to Monohydroxylated Building Blocks". Molecules 25, n.º 23 (7 de diciembre de 2020): 5764. http://dx.doi.org/10.3390/molecules25235764.
Texto completoHain, Julia, Patrick Rollin, Werner Klaffke y Thisbe K. Lindhorst. "Anomeric modification of carbohydrates using the Mitsunobu reaction". Beilstein Journal of Organic Chemistry 14 (29 de junio de 2018): 1619–36. http://dx.doi.org/10.3762/bjoc.14.138.
Texto completoWang, Ruibo, Kaimin Cai, Hua Wang, Chen Yin y Jianjun Cheng. "A caged metabolic precursor for DT-diaphorase-responsive cell labeling". Chemical Communications 54, n.º 38 (2018): 4878–81. http://dx.doi.org/10.1039/c8cc01715h.
Texto completode Robichon, Morgane, Andrea Bordessa, Maciej Malinowski, Jacques Uziel, Nadège Lubin-Germain y Angélique Ferry. "Access to C-aryl/alkenylglycosides by directed Pd-catalyzed C–H functionalisation of the anomeric position in glycal-type substrates". Chemical Communications 55, n.º 78 (2019): 11806–8. http://dx.doi.org/10.1039/c9cc05993h.
Texto completoSandoval, M., P. Hoyos, A. Cortés, T. Bavaro, M. Terreni y M. J. Hernáiz. "Development of regioselective deacylation of peracetylated β-d-monosaccharides using lipase from Pseudomonas stutzeri under sustainable conditions". RSC Adv. 4, n.º 98 (2014): 55495–502. http://dx.doi.org/10.1039/c4ra10401c.
Texto completoTesis sobre el tema "Anomeric position"
Hammoud, Jana. "Evaluation des complexes dirhodium (II) tétraacétate-Carbène-N-Hétérocyclique pour la décomposition de diazoesters et applications en glycochimie Functionalization of GlucoPyranosides at position 5 by 1,5 C–H insertion of Rh(II)-Carbenes: Dramatic influence of the anomeric configuration". Thesis, Normandie, 2020. http://www.theses.fr/2020NORMIR03.
Texto completoThis work deals with the study of the catalytic properties of Rh₂L₄.NHC complexes towards diazoesters, and their application in the field of glycochemistry. We first developed a reproducible synthetic procedure for the preparation of these organometallic complexes. Furthermore, we have shown that the Rh₂(OAC)₄.IMes complexe was inducing the chemoselective decomposition of diazo esters, depending on their electronic properties. This unprecedented property opened the way to a switchable catalytic system. In the field of glycochemistry, the Rh₂L₄.NHC complexes made possible to improve the experimental conditions for the quaternization reaction of the anomeric position by C-H bond functionalization. Finally, the quaternization of position 5 of pyranosides by 1,5 C-H insertion of a Rh (II) metallo-carbene anchored on the primary position was developed
Gavel, Marine. "Nouveaux développements chimiques pour la conception d'inhibiteurs de glycosyltransférases Carbene-mediated quaternarization of the anomeric position of carbohydrates: synthesis of allylic ketopyranosides, access to the missing α-gluco and β-manno stereoisomers, and preparation of quaternary 2-deoxy 2-acetamido sugars Regio- and chemoselective deprotection of primary acetates by zirconium hydrides". Thesis, Normandie, 2019. http://www.theses.fr/2019NORMIR09.
Texto completoThe goal of this project is to challenge the hypothesis that a non-natural sugar with a quaternary anomeric position might be the central core of a powerful and selective inhibitor of glycosyltransferase. Our design is relying on a key quaternary anomeric centre that provide the unique opportunity to incorporate in a single innovative structure the acceptor, the donor and the leaving group released during the formation of the glycosidic linkage. The functionnalization of the ketopyranosides that will be at the centre of this new class of potent glycosyltransferases inhibitors rely on original synthetic methods allowing introduction of a trimethylene phosphonate and regioselective deprotection of primary position of acetylated sugars for building alpha-1,6 glycosidic linkages
Capítulos de libros sobre el tema "Anomeric position"
Mébarki, K., M. Gavel, A. Joosten, T. Lecourt y F. Heis. "Carbene-Mediated Quaternarization of the Anomeric Position of Carbohydrates". En Carbohydrate Chemistry, 75–86. Boca Raton : CRC Press, 2020. | Series: Proven synthetic methods ; volume 5: CRC Press, 2021. http://dx.doi.org/10.1201/9781351256087-11.
Texto completoFrey, Perry A. y Adrian D. Hegeman. "Glycosyl Group Transferases". En Enzymatic Reaction Mechanisms. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195122589.003.0016.
Texto completoDavis, Benjamin G. y Antony J. Fairbanks. "Chemical disaccharide formation". En Carbohydrate Chemistry. Oxford University Press, 2002. http://dx.doi.org/10.1093/hesc/9780198558330.003.0007.
Texto completoDavid, Serge. "ABH and related blood group antigens". En The Molecular and Supramolecular Chemistry of Carbohydrates: Chemical Introduction to the Glycosciences, 265–76. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198500476.003.0016.
Texto completoDavid, Serge. "Conformation of monosaccharides and their derivatives". En The Molecular and Supramolecular Chemistry of Carbohydrates: Chemical Introduction to the Glycosciences, 17–41. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198500476.003.0002.
Texto completoMichalski, Jean-Claude y Catherine Alonso. "HPLC of oligosaccharides and glycopeptides". En HPLC of Macromolecules, 171–202. Oxford University PressOxford, 1998. http://dx.doi.org/10.1093/oso/9780199635719.003.0007.
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