Gotowe bibliografie tematyczne / Glycosidic bonds

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji

Gotowa bibliografia na temat „Glycosidic bonds”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 19 lutego 2022

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Artykuły w czasopismach na temat "Glycosidic bonds"

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Wang, Qian, Chao Gao, Nan Yang, and Katsuyoshi Nishinari. "Effect of simulated saliva components on the in vitro digestion of peanut oil body emulsion." RSC Advances 11, no. 49 (2021): 30520–31. http://dx.doi.org/10.1039/d1ra03274g.

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Joseleau, Jean-Paul, and Rachid Kesraoui. "Glycosidic Bonds between Lignin and Carbohydrates." Holzforschung 40, no. 3 (January 1986): 163–68. http://dx.doi.org/10.1515/hfsg.1986.40.3.163.

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Johnson, Glenn P., Luis Petersen, Alfred D. French, and Peter J. Reilly. "Twisting of glycosidic bonds by hydrolases." Carbohydrate Research 344, no. 16 (November 2009): 2157–66. http://dx.doi.org/10.1016/j.carres.2009.08.011.

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Khalilova, Gulnoza Abduvakhobovna, Abbaskhan Sabirkhanovich Turaev, Bahtiyor Ikromovich Muhitdinov, Albina Vasilevna Filatova, Saidakhon Bokijonovna Haytmetova та Nodirali Sokhobatalievich Normakhamatov. "Research On The Composition And Structure Of Β -Glucans Isolated From Basidiomycete Raw Materials Inonotus Hispidus". American Journal of Applied sciences 03, № 01 (19 січня 2021): 9–17. http://dx.doi.org/10.37547/tajas/volume03issue01-03.

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This article highlights the conducted researches on the composition and structure of β-glucans isolated from the basidiomycete raw material Inonotus hispidus. By means of using the alditol acetate method, as well as by UV and IR methods, one-dimensional (13C NMR, 1H NMR), two-dimensional (1H-1H COSY, 1H-13C HSQC) NMR spectroscopy, the composition and molecular structure of polysaccharides were determined and their branching was proved. It was clarified that the composition of the polysaccharide fractions consists mainly of glucose residues (68-100%), as well as residues of fructose, xylose, ma
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Weignerová, Lenka, Yukio Suzuki, Zdenka Huňková, Petr Sedmera, Vladimír Havlíček, Radek Marek, and Vladimír Křen. "Pyridoxine as a Substrate for Screening Synthetic Potential of Glycosidases." Collection of Czechoslovak Chemical Communications 64, no. 8 (1999): 1325–34. http://dx.doi.org/10.1135/cccc19991325.

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The reactions of glycosidases with pyridoxine were used for testing their ability to make new glycosidic bonds. Of 35 glycosidases examined, some exhibited regiospecificity towards one primary alcoholic group; glycosylation of phenolic hydroxyl group was not observed. A series of new glycosides of pyridoxine, 2-acetamido-2-deoxy-β-D-glucopyranosides, α-D-manno- pyranosides, and one α-D-galactopyranoside were prepared and completely characterized by MS and NMR.
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Kobayashi, Hirokazu, Yusuke Suzuki, Takuya Sagawa, Kyoichi Kuroki, Jun-ya Hasegawa, and Atsushi Fukuoka. "Impact of tensile and compressive forces on the hydrolysis of cellulose and chitin." Physical Chemistry Chemical Physics 23, no. 30 (2021): 15908–16. http://dx.doi.org/10.1039/d1cp01650d.

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Frański, R., P. Bednarek, D. Siatkowska, P. Wojtaszek, and M. Stobiecki. "Application of mass spectrometry to structural identification of flavonoid monoglycosides isolated from shoot of lupin (Lupinus luteus L.)." Acta Biochimica Polonica 46, no. 2 (June 30, 1999): 459–73. http://dx.doi.org/10.18388/abp.1999_4177.

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Flavonoid glycosides constitute important group of plant secondary metabolites. This class of natural products play significant role in different physiological processes. A new methodological approach where mass spectrometric techniques are applied to structural studies of this class of compounds is presented. Four flavonoid O-monoglycosides and one C-monoglycoside were isolated from green parts of lupin (Lupinus luteus L.). Several different mass spectrometric techniques were applied to structural elucidation of isolated compounds. Desorption ionization mass spectrometry was used for registra
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He, Xingxing, Fuyuan Zhang, Jifeng Liu, Guozhen Fang, and Shuo Wang. "Homogenous graphene oxide-peptide nanofiber hybrid hydrogel as biomimetic polysaccharide hydrolase." Nanoscale 9, no. 45 (2017): 18066–74. http://dx.doi.org/10.1039/c7nr06525f.

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Davies, Gideon J., Simon J. Charnock, and Bernard Henrissat. "The Enzymatic Synthesis of Glycosidic Bonds: "Glycosynthases" and Glycosyltransferases." Trends in Glycoscience and Glycotechnology 13, no. 70 (2001): 105–20. http://dx.doi.org/10.4052/tigg.13.105.

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Ibatullin, Farid M., Alexander M. Golubev, Leonid M. Firsov, and Kirill N. Neustroev. "A model for cleavage ofO-glycosidic bonds in glycoproteins." Glycoconjugate Journal 10, no. 3 (June 1993): 214–18. http://dx.doi.org/10.1007/bf00702202.

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Rozprawy doktorskie na temat "Glycosidic bonds"

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Baker, Anne. "The chemo-enzymatic synthesis of glycosidic bonds." Thesis, University of Exeter, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294484.

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Webberley, Matthew Christian. "The stereospecific synthesis of glycosidic bonds using glycosidases." Thesis, University of Exeter, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303771.

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Henderson, Margaret Esther. "Mechanisms of alkaline glycosidic bond cleavage in 1,5-anhydro-4-O-." Diss., Georgia Institute of Technology, 1986. http://hdl.handle.net/1853/5744.

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Deshpande, Sagar Nandkumar. "Pre-hydrolysis of the Phenyl Glycosidic Bond in a Model Compound." Fogler Library, University of Maine, 2008. http://www.library.umaine.edu/theses/pdf/DeshpandeSN2008.pdf.

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Tennant-Eyles, Richard J. "Peptide templated oligosaccharide synthesis : a novel strategy for glycosidic bond formation." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365751.

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Collins, James P. "Prebiotic Synthesis of Pyrimidine Nucleosides." Thesis, Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/14095.

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The problem of forming a glycosidic bond between ribose and the free nucleoside bases to produce beta-nucleosides under plausible prebiotic conditions is commonly referred to in origin of life research as The Nucleoside Problem. The lack of a general solution to this problem currently represents one of the largest stumbling blocks to the RNA world hypothesis and many other theories regarding the origin of life. Over thirty years ago the purine nucleosides were successfully synthesized by drying the fully-formed bases and ribose together in the presence of divalent metal ion salts. However, gly
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Molinarolo, William E. "The high temperature alkaline degradation of phenyl β-D-glucopyranoside". Diss., Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/5753.

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Callam, Christopher Stephen. "Experimental and Theoretical Studies of: Methyl 4a-carba-D-arabinofuranosides and 2,3-Anydrosugars in Glycoside Bond Synthesis." The Ohio State University, 2003. http://rave.ohiolink.edu/etdc/view?acc_num=osu1048691172.

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Mendoza, Muñoz María Fernanda. "Estudios teóricos y computacionales para la síntesis enzimática del enlace glicosídico." Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/400072.

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En esta tesis se ha investigado el mecanismo catalítico de las glicosiltransferasas que retienen la configuración a través de simulaciones híbridas de mecánica cuántica/mecánica molecular (QM/MM) y dinámicas moleculares (MD). La investigación se centra en la evaluación de las propuestas mecanísticas, además de la identificación de los principales factores que contribuyen a la eficiencia catalítica. Para esto usamos dos enzimas, α1,4-N-Acetilhexosaminiltransferasa (EXTL2) y Glucosil-3-fosfoglicerato Sintasa (GpgS) de Mycobacterium Tuberculosis. Además, se llevaron a cabo simulaciones adicionale
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Bruneau, Alexandre. "Développement de nouvelles réactions métallo-catalysées pour la création de liaisons C-C et C-hétéroatomes : Application à la synthèse d’inhibiteurs de la Hsp90 et aux ligands de la lectine A." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS138.

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Les travaux rapportés dans ce mémoire concernent le développement de nouvelles réactions métallo-catalysées pour la création de liaison carbone-hétéroatome et carbone-carbone ainsi que leurs applications à la synthèse de produits biologiquement actifs. La première partie de ce manuscrit est consacrée à l'étude de la réactivité des sucres dans les couplages organométalliques. Des conditions ont été développées pour la création de la liaison C-S entre glycosyl thiols et partenaires arylés. De plus, la création de la liaison carbone azote de glycosyl amines avec des acides boroniques a été étudié
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Książki na temat "Glycosidic bonds"

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Henderson, Margaret Esther. Mechanisms of alkaline glycosidic bond cleavage in 1,5-anhydro-4-O- -mannopyranosyl-D-mannitol. 1986.

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Części książek na temat "Glycosidic bonds"

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Monti, Daniela, and Sergio Riva. "Hydrolysis and Formation of Glycosidic Bonds." In Enzyme Catalysis in Organic Synthesis, 417–66. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch10.

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Pinto, José-Henrique Q., Zin-Eddine Dadach, Alain Lemoyne, and Serge Kaliaguine. "Acid Hydrolysis of Glycosidic Bonds in Polysaccharides: Modelling and Stochastic Simulation." In Advances in Thermochemical Biomass Conversion, 1583–97. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1336-6_129.

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Gooch, Jan W. "Glycosidic Bond." In Encyclopedic Dictionary of Polymers, 896. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13849.

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Pengelly, Andrew. "Glycosides." In The constituents of medicinal plants, 59–72. 3rd ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0004.

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Abstract Glycosides are a group of compounds consisting of a sugar portion (or moiety) attached by a special bond to one or more non-sugar portions. Chemically, they are hydroxyls of a sugar capable of forming ethers with other alcohols, or esters with acids. This chapter provides information on glycosides, including their distribution throughout the plant kingdom, medicinal properties, and toxicity.
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Miljković, Momčilo. "Chemistry of the Glycosidic Bond." In Carbohydrates, 323–421. New York, NY: Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-92265-2_12.

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Aharoni, Amir, and Stephen G. Withers. "Screening Methodologies for Glycosidic Bond Formation." In Protein Engineering Handbook, 605–20. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634026.ch25.

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Ye, Xin-Shan, and Weigang Lu. "GENERAL ASPECTS IN O-GLYCOSIDIC BOND FORMATION." In Glycochemical Synthesis, 69–95. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119006435.ch3.

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Miljkovic, Momcilo. "Armed-Disarmed Concept in the Synthesis of Glycosidic Bond." In Electrostatic and Stereoelectronic Effects in Carbohydrate Chemistry, 117–79. Boston, MA: Springer US, 2013. http://dx.doi.org/10.1007/978-1-4614-8268-0_5.

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Schmidt, Richard R., Simon Jonke, and Ke-gang Liu. "New Aspects of Glycoside Bond Formation: Solid-Phase Oligosaccharide Synthesis." In ACS Symposium Series, 209–36. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0960.ch013.

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Priebe, Waldemar, Piotr Skibicki, Oscar Varela, Nouri Neamati, Marcos Sznaidman, Krzysztof Dziewiszek, Grzegorz Grynkiewicz, et al. "Non-Cross-Resistant Anthracyclines with Reduced Basicity and Increased Stability of the Glycosidic Bond." In ACS Symposium Series, 14–46. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1995-0574.ch002.

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Streszczenia konferencji na temat "Glycosidic bonds"

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Withers, Stephen G. "ENZYMATIC CLEAVAGE AND FORMATION OF GLYCOSIDIC BONDS: FROM GLYCOSIDASES AND LYASES TO TRANSFERASES AND GLYCOSYNTHASES." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.355.

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Rodgers, M., Jos Oomens, Giel Berden, Chase Leslie, Erik Soley, Harrison Roy, Zachary Devereaux, et al. "INFLUENCE OF NATURALLY-OCCURRING AND SYNTHETIC MODIFICATIONS ON THE STRUCTURES AND GLYCOSIDIC BOND STABILITIES OF DNA AND RNA NUCLEOSIDES." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.ma02.

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