Literatura académica sobre el tema "Allyl glycosides"
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Artículos de revistas sobre el tema "Allyl glycosides"
Pal, Rita, Anupama Das y Narayanaswamy Jayaraman. "One-pot oligosaccharide synthesis: latent-active method of glycosylations and radical halogenation activation of allyl glycosides". Pure and Applied Chemistry 91, n.º 9 (25 de septiembre de 2019): 1451–70. http://dx.doi.org/10.1515/pac-2019-0306.
Texto completoGibson, Robin R., Roger P. Dickinson y Geert-Jan Boons. "Vinyl glycosides in oligosaccharide synthesis (part 4): glycosidase-catalysed preparation of substituted allyl glycosides". Journal of the Chemical Society, Perkin Transactions 1, n.º 22 (1997): 3357–60. http://dx.doi.org/10.1039/a704703g.
Texto completoKrähmer, Ralf, Lothar Hennig, Matthias Findeisen, Dietrich Müller y Peter Welzel. "Oxidative deprotection of allyl glycosides". Tetrahedron 54, n.º 36 (septiembre de 1998): 10753–60. http://dx.doi.org/10.1016/s0040-4020(98)00640-1.
Texto completoSherman, Andrei A., Leonid O. Kononov, Alexander S. Shashkov, Georgij V. Zatonsky y Nikolay E. Nifant’ev. "Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides". Mendeleev Communications 8, n.º 1 (enero de 1998): 9–11. http://dx.doi.org/10.1070/mc1998v008n01abeh000887.
Texto completoWang, Pengfei, Pranab Haldar, Yun Wang y Huayou Hu. "Simple Glycosylation Reaction of Allyl Glycosides". Journal of Organic Chemistry 72, n.º 15 (julio de 2007): 5870–73. http://dx.doi.org/10.1021/jo070512x.
Texto completoTimmer, Mattie S. M., Marta Vinciano Chumillas, Wilma E. Donker‐Koopman, Johannes M. F. G. Aerts, Gijsbert A. van derMarel, Herman S. Overkleeft y Jacques H. van Boom. "Selective Cross‐Metathesis ofC‐Allyl‐Glycosides". Journal of Carbohydrate Chemistry 24, n.º 4-6 (agosto de 2005): 335–51. http://dx.doi.org/10.1080/07328300500174887.
Texto completoGIBSON, R. R., R. P. DICKINSON y G. J. BOONS. "ChemInform Abstract: Vinyl Glycosides in Oligosaccharide Synthesis. Part 4. Glycosidase-Catalyzed Preparation of Substituted Allyl Glycosides." ChemInform 29, n.º 14 (23 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199814171.
Texto completoHu, Yun-Jin, Romyr Dominique, Sanjoy Kumar Das y René Roy. "A facile new procedure for the deprotection of allyl ethers under mild conditions". Canadian Journal of Chemistry 78, n.º 6 (1 de junio de 2000): 838–45. http://dx.doi.org/10.1139/v00-073.
Texto completoKRAEHMER, R., L. HENNIG, M. FINDEISEN, D. MUELLER y P. WELZEL. "ChemInform Abstract: Oxidative Deprotection of Allyl Glycosides." ChemInform 29, n.º 50 (18 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199850242.
Texto completoSHERMAN, A. A., L. O. KONONOV, A. S. SHASHKOV, G. V. ZATONSKY y N. E. NIFANT'EV. "ChemInform Abstract: Synthesis of Spacer-Armed Glycosides Using Azidophenylselenylation of Allyl Glycosides." ChemInform 29, n.º 30 (20 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199830240.
Texto completoTesis sobre el tema "Allyl glycosides"
Cumpstey, Ian. "The stereospecific formation of 1,2-cis glycosides via allyl-mediated intramolecular aglycon delivery". Thesis, University of Oxford, 2002. http://ora.ox.ac.uk/objects/uuid:2c4e0fb3-5a43-473a-bfbb-43557f19ffe9.
Texto completoFoucart, Quentin. "Etude de la débenzylation régiosélective en position 2 de 1-C-allyl iminosucres pour l'introduction de diversité moléculaire". Thesis, Poitiers, 2018. http://www.theses.fr/2018POIT2318.
Texto completoIminosugars constitute undoubtedly the most promising class of sugar analogues, their unique glycosidase and/or glycosyltransferase inhibition profile making them promising therapeutics. To generate more potent and selective inhibitors called C-glycoside iminosugars, introduction of a stable pseudoanomeric substituent is usually performed, the improved efficacy being attributed in part to the information brought by the aglycon moiety.The main challenge associated with this class of iminosugars C-glycosides is currently the design of efficient and general routes enabling introduction of structural diversity at a late stage from advanced synthons to accelerate the discovery of biologically relevant molecules. In this context, we have explored a strategy based on a regioselective debenzylation at C-2 and a stereocontrolled nucleophilic substitution assisted by the N-benzyl group. We have successfully applied this methodology on the C-allyl-1-deoxynojirimycin and extended it to several iminosugars in the piperidine and pyrrolidine series.The introduction of molecular diversity was performed from the C-allyl-1-deoxynojirimycin selectively O-debenzylated at position 2. We obtained several iminosugars in the D-gluco- and D-manno- series bearing various functionalities at position 2. This strategy allowed us to access a wide range of C-allyl iminosugars from one single synthon. We have also described the access to unknown bicyclic iminosugars starting from a C-allyl 2-keto iminosugar obtained by our regioselective debenzylative methodology
Bai, Yu. "A latent-active glycosylation approach for the synthesis of saccharides derived from the capsular polysaccharide of group B Streptococcus type IA". Thesis, University of Birmingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343849.
Texto completoMilkereit, Götz Eckart. "Investigation of colloidal, biophysical and liquid crystalline properties of synthetic alkyl glycosides and glycolipids". [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980736676.
Texto completoChabaud, Laurent. "Carboazidation d'allylsilanes chiraux : application à la synthèse totale d'alcaloïdes polyhydroxyles inhibiteurs de glycosidases". Bordeaux 1, 2005. http://www.theses.fr/2005BOR13040.
Texto completoBayle, Corinne. "Mise au point d'une méthode d'éthérification sélective en série osidique : étude par résonance magnétique nucléaire des molécules amphiphiles synthétisées". Université Joseph Fourier (Grenoble), 1994. http://www.theses.fr/1994GRE10139.
Texto completoDaskhan, Gour Chand. "C-2 And C-4 Branched Carbohydrates : (i) Synthesis And Studies Of Oligosacchardes With Expanded Glycosidic Linkage At C-4; (ii) Synthesis Of 2-Deoxy-2-C-Alkyl Glycopyranosides". Thesis, 2012. http://etd.iisc.ernet.in/handle/2005/2462.
Texto completo張元軍. "Synthesis of N-alkyl Iminoalditol and pyrrolidine derivatives as Glycosidase Inhibitors". Thesis, 2009. http://ndltd.ncl.edu.tw/handle/83759606820380930634.
Texto completo國立彰化師範大學
化學系
97
The goals of our research are to synthesize glycosidase inhibitors. The first project is using D-ribose as starting material to synthesize the derivatives of ribopyranoside. We are successful to obtain the target compound methyl 2-C-(5-deoxy-2,3-di-O-isopropylidene-5 morpholinopropylamino-β-D-ribopyranosyl) acetate 7, methyl 2-C-(5-deoxy-2,3-di-O-isopropylidene-5-decylamino-β-Dribopyranosyl) acetate 9, 2-C-(5-deoxy-2,3-di-O-isopropylidene-5-morpholinopropyl amino-β-D-ribopyranosyl)ethanol 8, and 2-C-(5-deoxy-2,3-di-O-isopropylidene-5- decylamino -β-D-ribopyranosyl)ethanol 10 as shown in figure 1. The second project is using dimesylate as the starting materials to synthesize the derivatives of pyrrolidine. This study shows that amination reactions of dimesylate with various alkylamines can be substantially improved by microwave heating. This approach shortens reaction times from 1.5-72 h to 10-30 min and the yields are also improved. We are successful to obtain the target compound 1,2-bis-(2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-imino- L-ribitol-1-yl)ethane 21, bis(2-(2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-imino-L-ribitol-1-yl)ethyl)amine 22, and 1-(2-(2,3,5-Tri-O-benzyl-1,4-dideoxy-1,4-imino-L-ribitol-1- yl)ethyl)-4-((2,3,5-tri-O-benzyl-1,4-dideoxy-1,4-imino-L-ribitol-1-yl)methyl)-1H-1,2,3-triazole 26 as shown in figure 1.
Milkereit, Götz Eckart [Verfasser]. "Investigation of colloidal, biophysical and liquid crystalline properties of synthetic alkyl glycosides and glycolipids / vorgelegt von Götz Eckart Milkereit". 2006. http://d-nb.info/980736676/34.
Texto completoMukherjee, Arunima. "Studies On 2,3-Unsaturated Sugars : Reactivity Switching, Rearrangements And Conjugate Additions". Thesis, 2012. http://hdl.handle.net/2005/2500.
Texto completoLibros sobre el tema "Allyl glycosides"
Hoffmann, Michael G. O-Glycosylimidate zur Synthese von funktionell substituierten Alkyl-C-glycosiden. Konstanz: Hartung-Gorre, 1985.
Buscar texto completoDieter, Balzer y Lüders Harald, eds. Nonionic surfactants: Alkyl polyglucosides. New York: Marcel Dekker, 2000.
Buscar texto completoPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2014.
Buscar texto completoPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2014.
Buscar texto completoPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2018.
Buscar texto completo(Editor), Dieter Balzer y Harald Luders (Editor), eds. Nonionic Surfactants: Alkyl Polyglucosides (Surfactant Science). CRC, 2000.
Buscar texto completoAkoh, Casimir Chike. Synthesis and properties of carbohydrate and alkyl glycoside fatty acid polyesters: Low calorie oil and fat substitutes. 1988.
Buscar texto completoCapítulos de libros sobre el tema "Allyl glycosides"
Kryczka, B., J. Lewkowski y A. Zawisza. "1--Allyl Glycosides". En Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00964.
Texto completoKryczka, B., J. Lewkowski y A. Zawisza. "Formation of 1--Allyl Glycosides". En Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00948.
Texto completoKryczka, B., J. Lewkowski y A. Zawisza. "Isomerization of 1--Allyl Glycosides". En Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00960.
Texto completoTaber, Douglass. "C-O Ring Natural Products: (-)-Serotobenine (Fukuyama-Kan), (-)-Aureonitol (Cox), Salmochelin SX (Gagné), Botcinin F (Shiina), (-)-Saliniketal B (Paterson), Haterumalide NA (Borhan)". En Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0051.
Texto completoGunn, S. J., S. L. Warriner y J. W. White. "Synthesis from -Alkyl Glycosides". En Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00808.
Texto completo"3. Alkyl et aryl glycosides. Glycosylamines". En Chimie moléculaire et supramoléculaire des sucres, 45–70. EDP Sciences, 1995. http://dx.doi.org/10.1051/978-2-7598-0267-8.c004.
Texto completoPostema, Maarten H. D. "Synthesis of Alkyl C-Glycoside Natural Products". En C-Glycoside Synthesis, 227–64. CRC Press, 2020. http://dx.doi.org/10.1201/9781003069249-9.
Texto completo"Solution Behavior of Alkyl Glycosides and Related Compounds". En Sugar-Based Surfactants, 41–80. CRC Press, 2008. http://dx.doi.org/10.1201/9781420051674-6.
Texto completoAndreozzi, Patrizia, Giacomo Gente y Camillo La Mesa. "Solution Behavior of Alkyl Glycosides and Related Compounds". En Surfactant Science. CRC Press, 2008. http://dx.doi.org/10.1201/9781420051674.ch2.
Texto completoVanaken, T., S. Foxall-Vanaken, S. Castleman y S. Ferguson-Miller. "[3] Alkyl glycoside detergents: Synthesis and applications to the study of membrane proteins". En Methods in Enzymology, 27–35. Elsevier, 1986. http://dx.doi.org/10.1016/s0076-6879(86)25005-3.
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