Pure and Applied Chemistry

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• Vilcocq Léa, Castilho Paula C., Carvalheiro Florbela, Duarte Luís C.: Hydrolysis of Oligosaccharides Over Solid Acid Catalysts: A Review. ChemSusChem 2014, 7, 1010. <http://dx.doi.org/10.1002/cssc.201300720>
• Villalonga María L., Díez Paula, Sánchez Alfredo, Gamella María, Pingarrón José M., Villalonga Reynaldo: Neoglycoenzymes. Chem. Rev. 2014, 140204133705006. <http://dx.doi.org/10.1021/cr400290x>
• Mayes Heather B., Broadbelt Linda J., Beckham Gregg T.: How Sugars Pucker: Electronic Structure Calculations Map the Kinetic Landscape of Five Biologically Paramount Monosaccharides and Their Implications for Enzymatic Catalysis. J. Am. Chem. Soc. 2014, 136, 1008. <http://dx.doi.org/10.1021/ja410264d>
• Pol-Fachin L., Verli H.: Structural glycobiology of heparin dynamics on the exosite 2 of coagulation cascade proteases: Implications for glycosaminoglycans antithrombotic activity. Glycobiology 2014, 24, 97. <http://dx.doi.org/10.1093/glycob/cwt095>
• Li Haichen, Qiao Yuanyuan: Bimolecular nature of boron trifluoride catalyzed glycosylation of a galactosyl donor: The role of the acceptor. Int. J. Quantum Chem. 2013, 113, 1975. <http://dx.doi.org/10.1002/qua.24422>
• Steiner Bohumil, Langer Vratislav, Bella Maroš, Koóš Miroslav: Cyanohydrins from methyl 6-deoxy-2,3-O-isopropylidene-α-l-lyxo-hexofuranosid-4-ulose via Bucherer–Bergs and Strecker reactions. Carbohydrate Research 2013, 369, 31. <http://dx.doi.org/10.1016/j.carres.2012.09.008>
• Chiodi Carla G., Verli Hugo: Structural characterization of NETNES glycopeptide from Trypanosoma cruzi. Carbohydrate Research 2013, 373, 28. <http://dx.doi.org/10.1016/j.carres.2013.03.010>
• Rönsberg David, Debbab Abdessamad, Mándi Attila, Wray Victor, Dai Haofu, Kurtán Tibor, Proksch Peter, Aly Amal H.: Secondary metabolites from the endophytic fungus Pestalotiopsis virgatula isolated from the mangrove plant Sonneratia caseolaris. Tetrahedron Letters 2013, 54, 3256. <http://dx.doi.org/10.1016/j.tetlet.2013.04.031>
• Mallick Asadulla, John Pal A.P., Vankar Yashwant D.: Synthesis of l-3-epi-isofagomine, its homo-, n-butyl and bicyclic analogues from d-glucose as glycosidase inhibitors. Tetrahedron Letters 2013, 54, 6549. <http://dx.doi.org/10.1016/j.tetlet.2013.09.102>
• Virgens Madza Yasodara Farias, Pol-Fachin Laercio, Verli Hugo, Saraiva-Pereira Maria Luiza: Effects of glycosylation and pH conditions in the dynamics of human arylsulfatase A. Journal of Biomolecular Structure and Dynamics 2013, 1. <http://dx.doi.org/10.1080/07391102.2013.780982>
• Li Yangbing, Yin Zhaojun, Wang Bo, Meng Xiang-Bao, Li Zhong-Jun: Synthesis of orthogonally protected l-glucose, l-mannose, and l-galactose from d-glucose. Tetrahedron 2012, 68, 6981. <http://dx.doi.org/10.1016/j.tet.2012.04.001>
• Ghadban Ali, Albertin Luca, Rinaudo Marguerite, Heyraud Alain: Biohybrid Glycopolymer Capable of Ionotropic Gelation. Biomacromolecules 2012, 13, 3108. <http://dx.doi.org/10.1021/bm300925j>
• Pol-Fachin Laercio, Rusu Victor H., Verli Hugo, Lins Roberto D.: GROMOS 53A6GLYC, an Improved GROMOS Force Field for Hexopyranose-Based Carbohydrates. J. Chem. Theory Comput. 2012, 8, 4681. <http://dx.doi.org/10.1021/ct300479h>
• Manickam Achari Vijayan, Nguan Hock Seng, Heidelberg Thorsten, Bryce Richard A., Hashim Rauzah: Molecular Dynamics Study of Anhydrous Lamellar Structures of Synthetic Glycolipids: Effects of Chain Branching and Disaccharide Headgroup. J. Phys. Chem. B 2012, 116, 11626. <http://dx.doi.org/10.1021/jp302292s>
• Pedebos Conrado, Pol-Fachin Laercio, Verli Hugo: Unrestrained Conformational Characterization of Stenocereus eruca Saponins in Aqueous and Nonaqueous Solvents. J. Nat. Prod. 2012, 75, 1196. <http://dx.doi.org/10.1021/np3000393>
• Merino-Montiel Penélope, López Óscar, Fernández-Bolaños José G.: Unprecedented spiro-annelated sugar isoureas, guanidines and amidines as new families of glycosidase inhibitors. RSC Adv. 2012, 2, 11326. <http://dx.doi.org/10.1039/c2ra21561f>
• Pol-Fachin L., Verli H.: Structural glycobiology of the major allergen of Artemisia vulgaris pollen, Art v 1: O-glycosylation influence on the protein dynamics and allergenicity. Glycobiol 2012, 22, 817. <http://dx.doi.org/10.1093/glycob/cws056>
• Hansen Halvor S., Hünenberger Philippe H.: A reoptimized GROMOS force field for hexopyranose-based carbohydrates accounting for the relative free energies of ring conformers, anomers, epimers, hydroxymethyl rotamers, and glycosidic linkage conformers. J Comput Chem 2011, 32, 998. <http://dx.doi.org/10.1002/jcc.21675>
• Schulten Johanna, Klüfers Peter: Dibutylsilylene–pentose bis-chelates: on the glycoses’ binding sites for strongly Lewis-acidic centres. Carbohydrates Research 2011, 346, 1767. <http://dx.doi.org/10.1016/j.carres.2011.05.035>
• Ghadban Ali, Albertin Luca, Moussavou Mounguengui Rédéo W., Peruchon Alexandre, Heyraud Alain: Synthesis of β-d-glucopyranuronosylamine in aqueous solution: kinetic study and synthetic potential. Carbohydrates Research 2011, 346, 2384. <http://dx.doi.org/10.1016/j.carres.2011.08.018>
• Jamison Francis W., Foster Theresa J., Barker Jacob A., Hills Ronald D., Guvench Olgun: Mechanism of Binding Site Conformational Switching in the CD44–Hyaluronan Protein–Carbohydrate Binding Interaction. Journal of Molecular Biology 2011, 406, 631. <http://dx.doi.org/10.1016/j.jmb.2010.12.040>
• Ghadban Ali, Albertin Luca, Condamine Eric, Mounguengui Rédéo W. Moussavou, Heyraud Alain: NMR and MS study of the formation of β-d-glucopyranosylamine uronic acid in aqueous solution. Can J Chern 2011, 89, 987. <http://dx.doi.org/10.1139/v11-064>
• MCNAUGHT A. D.: ChemInform Abstract: Nomenclature of Carbohydrates. ChemInform 2010, 28, no. <http://dx.doi.org/10.1002/chin.199713308>
• Fernandes C.L., Sachett L.G., Pol-Fachin L., Verli H.: GROMOS96 43a1 performance in predicting oligosaccharide conformational ensembles within glycoproteins. Carbohydrates Research 2010, 345, 663. <http://dx.doi.org/10.1016/j.carres.2009.12.018>
• Perić-Hassler Lovorka, Hansen Halvor S., Baron Riccardo, Hünenberger Philippe H.: Conformational properties of glucose-based disaccharides investigated using molecular dynamics simulations with local elevation umbrella sampling. Carbohydrates Research 2010, 345, 1781. <http://dx.doi.org/10.1016/j.carres.2010.05.026>
• Pol-Fachin Laercio, Serrato Rodrigo V., Verli Hugo: Solution conformation and dynamics of exopolysaccharides from Burkholderia species. Carbohydrates Research 2010, 345, 1922. <http://dx.doi.org/10.1016/j.carres.2010.06.010>
• Barnett Christopher B., Wilkinson Karl A., Naidoo Kevin J.: Pyranose Ring Transition State Is Derived from Cellobiohydrolase I Induced Conformational Stability and Glycosidic Bond Polarization. J Am Chem Soc 2010, 132, 12800. <http://dx.doi.org/10.1021/ja103766w>
• Luo Hairong, Zou Wei, Shao Huawu: Synthesis of N-substituted iminosugars from 2′-carbonyl-C-glycofuranosides. Carbohydrates Research 2009, 344, 2454. <http://dx.doi.org/10.1016/j.carres.2009.08.024>
• Bosma Wayne B., Schnupf Udo, Willett J.L., Momany Frank A.: Density functional study of the infrared spectrum of glucose and glucose monohydrates in the OH stretch region. Journal of Molecular Structure: THEOCHEM 2009, 905, 59. <http://dx.doi.org/10.1016/j.theochem.2009.03.013>
• Nishimura Yoshio: Gem-diamine 1-N-iminosugars as versatile glycomimetics: synthesis, biological activity and therapeutic potential. J Antibiot 2009, 62, 407. <http://dx.doi.org/10.1038/ja.2009.53>
• Cui Qingzhou, Ward Muscatello Michelle M., Asher Sanford A.: Photonic crystal borax competitive binding carbohydrate sensing motif. Analyst 2009, 134, 875. <http://dx.doi.org/10.1039/b901017n>
• Fauré Régis, Courtin Christophe M., Delcour Jan A., Dumon Claire, Faulds Craig B., Fincher Geoffrey B., Fort Sébastien, Fry Stephen C., Halila Sami, Kabel Mirjam A.: A Brief and Informationally Rich Naming System for Oligosaccharide Motifs of Heteroxylans Found in Plant Cell Walls. Aust J Chem 2009, 62, 533. <http://dx.doi.org/10.1071/CH08458>
• Krambeck F. J, Bennun S. V, Narang S., Choi S., Yarema K. J, Betenbaugh M. J: A mathematical model to derive N-glycan structures and cellular enzyme activities from mass spectrometric data. Glycobiol 2009, 19, 1163. <http://dx.doi.org/10.1093/glycob/cwp081>
• Aguilar Matilde, Gloster Tracey M., García-Moreno M. Isabel, Ortiz Mellet Carmen, Davies Gideon J., Llebaria Amadeu, Casas Josefina, Egido-Gabás Meritxell, García Fernandez José M.: Molecular Basis for β-Glucosidase Inhibition by Ring-Modified Calystegine Analogues. Chem Eur J of Chem Bio 2008, 9, 2612. <http://dx.doi.org/10.1002/cbic.200800451>
• Louis Farida, García-Moreno M. Isabel, Balbuena Patricia, Mellet Carmen Ortiz, García Fernández José M.: Stereoselective synthesis of nonsymmetrical difructose dianhydrides from xylylene-tethered d-fructose precursors. Tetrahedron 2008, 64, 2792. <http://dx.doi.org/10.1016/j.tet.2008.01.054>
• Oelze Benjamin, Albert Dieter, Kirschning Andreas: Synthetic and structural studies on macrocyclic amino cyclitols – conformational chameleons. Org Biomol Chem 2008, 6, 2412. <http://dx.doi.org/10.1039/b716347a>
• Schnupf Udo, Willett J.L., Bosma Wayne B., Momany Frank A.: DFT study of α- and β-d-allopyranose at the B3LYP/6-311++G∗∗ level of theory. Carbohydrates Research 2007, 342, 196. <http://dx.doi.org/10.1016/j.carres.2006.12.006>
• García-Moreno M. Isabel, Mellet Carmen Ortiz, García Fernández José M.: Synthesis and biological evaluation of 6-oxa-nor-tropane glycomimetics as glycosidase inhibitors. Tetrahedron 2007, 63, 7879. <http://dx.doi.org/10.1016/j.tet.2007.05.085>
• Radha Krishna Palakodety, Narasimha Reddy P.V., Sreeshailam A., Uday Kiran M., Jagdeesh B.: The Baylis–Hillman reaction: a strategic tool for the synthesis of higher-carbon sugars. Tetrahetron Lett 2007, 48, 6466. <http://dx.doi.org/10.1016/j.tetlet.2007.07.067>
• Nakahara T., Hashimoto R., Nakagawa H., Monde K., Miura N., Nishimura S.-I.: Glycoconjugate Data Bank:Structures an annotated glycan structure database and N-glycan primary structure verification service. Nucleic Acids Res 2007, 36, D368. <http://dx.doi.org/10.1093/nar/gkm833>
• Guaragna Annalisa, Napolitano Carmela, D'Alonzo Daniele, Pedatella Silvana, Palumbo Giovanni: A Versatile Route to l-Hexoses:  Synthesis of l-Mannose and l-Altrose. Org Lett 2006, 8, 4863. <http://dx.doi.org/10.1021/ol061916z>
• Swennen Katrien, Courtin Christophe M., Delcour Jan A.: Non-digestible Oligosaccharides with Prebiotic Properties. Crit Rev Food Sci Nutrit 2006, 46, 459. <http://dx.doi.org/10.1080/10408390500215746>
• French Alfred D., Johnson Glenn P., Kelterer Anne-Marie, Csonka Gábor I.: Fluorinated cellobiose and maltose as stand-ins for energy surface calculations. Tet Asymm 2005, 16, 577. <http://dx.doi.org/10.1016/j.tetasy.2004.12.007>
• Livesey Geoffrey: Health potential of polyols as sugar replacers, with emphasis on low glycaemic properties. nutr res rev 2003, 16, 163. <http://dx.doi.org/10.1079/NRR200371>
• Koch T: Locked nucleic acids: a family of high affinity nucleic acid probes. J Phys Condens Matter 2003, 15, S1861. <http://dx.doi.org/10.1088/0953-8984/15/18/317>
• Boulineau Fabien P., Wei Alexander: Synthesis of l-Sugars from 4-Deoxypentenosides. Org Lett 2002, 4, 2281. <http://dx.doi.org/10.1021/ol026175q>
• Chester M.Alan: IUPAC-IUB joint commission on biochemical nomenclature (JCBN) nomenclature of glycolipids. Journal of Molecular Biology 1999, 286, 963. <http://dx.doi.org/10.1006/jmbi.1998.2485>
• Staaf Mikael, Weintraub Andrej, Widmalm Goran: Structure determination of the O-antigenic polysaccharide from the enteroinvasive Escherichia coli O136. Eur J Biochem 1999, 263, 656. <http://dx.doi.org/10.1046/j.1432-1327.1999.00531.x>
• Kraehenbuehl Karin, Picasso Sylviane, Vogel Pierre: Synthesis of C-Linked Imino Disaccharides (= Aza-C-disaccharides) with a Pyrrolidine-3,4-diol Moiety Attached at C(3) of Galactosevia a Hydroxymethylene Linker and of a 7-(1,2,3-Trihydroxypropyl)-octahydroxyindolizine-1,2,6,8-tetrol. HCA 1998, 81, 1439. <http://dx.doi.org/10.1002/hlca.19980810552>
• Bruno Ian J., Kemp Nick M., Artymiuk Peter J., Willett Peter: Representation and searching of carbohydrate structures using graph-theoretic techniques. Carbohydrates Research 1997, 304, 61. <http://dx.doi.org/10.1016/S0008-6215(97)00196-1>
• IUPAC-IUBMB Joint Commission on Biochemical Nomenclature (JCBN) Nomenclature of Carbohydrates. Recommendations 1996. Eur J Biochem 1997, 243, 9. <http://dx.doi.org/10.1111/j.1432-1033.1997.09_1a.x>