Добірка наукової літератури з теми "Allyl glycosides"
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Статті в журналах з теми "Allyl glycosides"
Pal, Rita, Anupama Das, and Narayanaswamy Jayaraman. "One-pot oligosaccharide synthesis: latent-active method of glycosylations and radical halogenation activation of allyl glycosides." Pure and Applied Chemistry 91, no. 9 (September 25, 2019): 1451–70. http://dx.doi.org/10.1515/pac-2019-0306.
Повний текст джерелаGibson, Robin R., Roger P. Dickinson, and 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, no. 22 (1997): 3357–60. http://dx.doi.org/10.1039/a704703g.
Повний текст джерелаKrähmer, Ralf, Lothar Hennig, Matthias Findeisen, Dietrich Müller, and Peter Welzel. "Oxidative deprotection of allyl glycosides." Tetrahedron 54, no. 36 (September 1998): 10753–60. http://dx.doi.org/10.1016/s0040-4020(98)00640-1.
Повний текст джерелаSherman, Andrei A., Leonid O. Kononov, Alexander S. Shashkov, Georgij V. Zatonsky, and Nikolay E. Nifant’ev. "Synthesis of spacer-armed glycosides using azidophenylselenylation of allyl glycosides." Mendeleev Communications 8, no. 1 (January 1998): 9–11. http://dx.doi.org/10.1070/mc1998v008n01abeh000887.
Повний текст джерелаWang, Pengfei, Pranab Haldar, Yun Wang, and Huayou Hu. "Simple Glycosylation Reaction of Allyl Glycosides." Journal of Organic Chemistry 72, no. 15 (July 2007): 5870–73. http://dx.doi.org/10.1021/jo070512x.
Повний текст джерелаTimmer, Mattie S. M., Marta Vinciano Chumillas, Wilma E. Donker‐Koopman, Johannes M. F. G. Aerts, Gijsbert A. van derMarel, Herman S. Overkleeft, and Jacques H. van Boom. "Selective Cross‐Metathesis ofC‐Allyl‐Glycosides." Journal of Carbohydrate Chemistry 24, no. 4-6 (August 2005): 335–51. http://dx.doi.org/10.1080/07328300500174887.
Повний текст джерелаGIBSON, R. R., R. P. DICKINSON, and G. J. BOONS. "ChemInform Abstract: Vinyl Glycosides in Oligosaccharide Synthesis. Part 4. Glycosidase-Catalyzed Preparation of Substituted Allyl Glycosides." ChemInform 29, no. 14 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199814171.
Повний текст джерелаHu, Yun-Jin, Romyr Dominique, Sanjoy Kumar Das, and René Roy. "A facile new procedure for the deprotection of allyl ethers under mild conditions." Canadian Journal of Chemistry 78, no. 6 (June 1, 2000): 838–45. http://dx.doi.org/10.1139/v00-073.
Повний текст джерелаKRAEHMER, R., L. HENNIG, M. FINDEISEN, D. MUELLER, and P. WELZEL. "ChemInform Abstract: Oxidative Deprotection of Allyl Glycosides." ChemInform 29, no. 50 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199850242.
Повний текст джерелаSHERMAN, A. A., L. O. KONONOV, A. S. SHASHKOV, G. V. ZATONSKY, and N. E. NIFANT'EV. "ChemInform Abstract: Synthesis of Spacer-Armed Glycosides Using Azidophenylselenylation of Allyl Glycosides." ChemInform 29, no. 30 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199830240.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаFoucart, 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.
Повний текст джерелаIminosugars 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.
Повний текст джерелаMilkereit, 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.
Повний текст джерелаChabaud, Laurent. "Carboazidation d'allylsilanes chiraux : application à la synthèse totale d'alcaloïdes polyhydroxyles inhibiteurs de glycosidases." Bordeaux 1, 2005. http://www.theses.fr/2005BOR13040.
Повний текст джерелаBayle, 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.
Повний текст джерелаDaskhan, 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.
Повний текст джерела張元軍. "Synthesis of N-alkyl Iminoalditol and pyrrolidine derivatives as Glycosidase Inhibitors." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/83759606820380930634.
Повний текст джерела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.
Повний текст джерелаMukherjee, Arunima. "Studies On 2,3-Unsaturated Sugars : Reactivity Switching, Rearrangements And Conjugate Additions." Thesis, 2012. http://hdl.handle.net/2005/2500.
Повний текст джерелаКниги з теми "Allyl glycosides"
Hoffmann, Michael G. O-Glycosylimidate zur Synthese von funktionell substituierten Alkyl-C-glycosiden. Konstanz: Hartung-Gorre, 1985.
Знайти повний текст джерелаDieter, Balzer, and Lüders Harald, eds. Nonionic surfactants: Alkyl polyglucosides. New York: Marcel Dekker, 2000.
Знайти повний текст джерелаPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2014.
Знайти повний текст джерелаPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2014.
Знайти повний текст джерелаPantelic, Ivana. Alkyl Polyglucosides: From Natural-Origin Surfactants to Prospective Delivery Systems. Elsevier Science & Technology, 2018.
Знайти повний текст джерела(Editor), Dieter Balzer, and Harald Luders (Editor), eds. Nonionic Surfactants: Alkyl Polyglucosides (Surfactant Science). CRC, 2000.
Знайти повний текст джерелаAkoh, Casimir Chike. Synthesis and properties of carbohydrate and alkyl glycoside fatty acid polyesters: Low calorie oil and fat substitutes. 1988.
Знайти повний текст джерелаЧастини книг з теми "Allyl glycosides"
Kryczka, B., J. Lewkowski, and A. Zawisza. "1--Allyl Glycosides." In 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.
Повний текст джерелаKryczka, B., J. Lewkowski, and A. Zawisza. "Formation of 1--Allyl Glycosides." In 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.
Повний текст джерелаKryczka, B., J. Lewkowski, and A. Zawisza. "Isomerization of 1--Allyl Glycosides." In 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.
Повний текст джерелаTaber, Douglass. "C-O Ring Natural Products: (-)-Serotobenine (Fukuyama-Kan), (-)-Aureonitol (Cox), Salmochelin SX (Gagné), Botcinin F (Shiina), (-)-Saliniketal B (Paterson), Haterumalide NA (Borhan)." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0051.
Повний текст джерелаGunn, S. J., S. L. Warriner, and J. W. White. "Synthesis from -Alkyl Glycosides." In 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.
Повний текст джерела"3. Alkyl et aryl glycosides. Glycosylamines." In Chimie moléculaire et supramoléculaire des sucres, 45–70. EDP Sciences, 1995. http://dx.doi.org/10.1051/978-2-7598-0267-8.c004.
Повний текст джерелаPostema, Maarten H. D. "Synthesis of Alkyl C-Glycoside Natural Products." In C-Glycoside Synthesis, 227–64. CRC Press, 2020. http://dx.doi.org/10.1201/9781003069249-9.
Повний текст джерела"Solution Behavior of Alkyl Glycosides and Related Compounds." In Sugar-Based Surfactants, 41–80. CRC Press, 2008. http://dx.doi.org/10.1201/9781420051674-6.
Повний текст джерелаAndreozzi, Patrizia, Giacomo Gente, and Camillo La Mesa. "Solution Behavior of Alkyl Glycosides and Related Compounds." In Surfactant Science. CRC Press, 2008. http://dx.doi.org/10.1201/9781420051674.ch2.
Повний текст джерелаVanaken, T., S. Foxall-Vanaken, S. Castleman, and S. Ferguson-Miller. "[3] Alkyl glycoside detergents: Synthesis and applications to the study of membrane proteins." In Methods in Enzymology, 27–35. Elsevier, 1986. http://dx.doi.org/10.1016/s0076-6879(86)25005-3.
Повний текст джерела