5 edition of Fluorinated Carbohydrates found in the catalog.
by Amer Chemical Society
Written in English
|The Physical Object|
|Number of Pages||214|
Contact information. Joseph Rodriguez [email protected]. Address: Tiptrans, Ste #, Slevacska /2A, Rumburk, Ustecky / Usti nad Labem, Czech Republic. Chemical synthesis of oligosaccharides. Great progress has been made in the chemical synthesis of complex carbohydrates, as demonstrated by the synthesis of sialic acid rich biantennary N-linked glycan 1 found in human Follicle-stimulating Hormone (hFSH) , sialyl Lewis x 2 , PIM glycans (such as PIM 6 3) from Mycobacterium tuberculosis , and the immuno-adjuvant QS-7 Cited by:
His research interests include the functionalization of fluorinated molecules by homogeneous catalysis taking into account their application in a bioorganic context. Johannes Kohlmann is a member of the Cluster of Excellence “Unifying Concepts in Catalysis” (UniCat) funded by the Deutsche by: Given the increasing interest in the biological roles of carbohydrates, recent advances in NMR can offer new insights into the functional understanding of carbohydrate interactions, which can overcome the challenge of developing new carbohydrate-derived therapeutics in the future.
Language: English ISBN: , LCCN: MeSH: Carbohydrates*; Fluorides* Publication Type(s): Congresses Notes: "Developed from a symposium sponsored by the Division of Carbohydrate Chemistry at the Meeting of the American Chemical Society, New Orleans, Louisiana, August September 4, ". Fluorine forms a great variety of chemical compounds, within which it always adopts an oxidation state of −1. With other atoms, fluorine forms either polar covalent bonds or ionic bonds. Most frequently, covalent bonds involving fluorine atoms are single bonds, although at least two examples of a higher order bond exist. Fluoride may act as a bridging ligand between two .
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Fluorinated Carbohydrates Chapter (PDF Available) in Advances in Organic Synthesis 2(1) - January with Reads How we measure 'reads'. Photochemical reactions of .etapentamethylcyclopentadienyl)dicarbonyliron alkyl and silyl complexes: reversible ethylene insertion into an iron-silicon bond and implications for the mechanism of transition-metal-catalyzed hydrosilation of alkenes.
Fluorinated carbohydrates, where one (or more) fluorine atom(s) have been introduced into a carbohydrate structure, typically through deoxyfluorination chemistry, have a wide range of applications in the glycosciences.
Fluorinated derivatives of galactose, glucose, N-acetylgalactosamine, N-acetylglucosamine, talose Glycosylation: New methodologies and.
Unraveling Sugar Binding Modes to DC-SIGN by Employing Fluorinated Carbohydrates by J. Daniel Martínez 1, Pablo Valverde 1, Sandra Delgado 1, Cecilia Romanò 2, Bruno Linclau 3, Niels C.
Reichardt 4,5, Stefan Oscarson 2, Ana Ardá 1, Jesús Jiménez-Barbero 1,6,7,* and F. Javier Cañada 8,*Cited by: 4. ISBN: OCLC Number: Language Note: English. Notes: "Developed from a symposium sponsored by the Division of Carbohydrate Chemistry at the meeting of the American Chemical Society, New Orleans.
Carbohydrate Chemistry – VI (Madison ) covers the proceedings of the Sixth International Symposium on Fluorinated Carbohydrates book Chemistry, held in Madison, USA on AugustChapter 1 focuses on the study of complex formation of sugar-metal complexes using proton magnetic resonance spectroscopy.
THE SYNTHESIS OF FLUORINATED CARBOHYDRATES A. FOSTER and J. W E S T W O O D Chester Beatty Research Institute, Fulham Road, London S.W.3, UK ABSTRACT Three types of reaction are of particular value in the synthesis of fluoro sugars, namely, nucleophilic displacements with fluoride salts, epoxide cleavage reactions, and glycal addition by: Intended for researchers in biochemistry, medicine, nutrition and industry, this book discusses such topics as components of bacterial polysaccharides, fluorinated carbohydrates, and carbon sugars chemistry.
Product Identifiers. Publisher. Elsevier Science & Technology Books. ISBN ISBN Title: Recent Progress in Synthesis and Applications of Fluorinated Carbohydrates VOLUME: 14 ISSUE: 9 Author(s):Yuan Cheng, Ai-Ling Guo and Dian-Shun Guo Affiliation:Department of Chemistry, Shandong Normal University, JinanP.
China. Abstract: The biological importance and activity of fluorinated carbohydrates is a focus of numerous investigations to Cited by: Fluorinated Carbohydrates. (49) Martin Hein and Ralf Miethchen. Abstract. The review demonstrates how carbohydrate chemists exploit the two fundamental strategies of organofluorine chemistry; (a) direct introduction of fluorine atom(s) or fluorinated groups by appropriate reagents in a late synthetic step, or (b) linking of fluorine-containing “building.
Lipophilicity is a much used parameter in drug development, and defined as the octanol-water partition coefficient. It is a measure for membrane permeability, and a proxy for solubility and ADME properties, which determine to a large degree dosing, and thus toxicity effects.
Get this from a library. Fluorinated carbohydrates: chemical and biochemical aspects: developed from a symposium sponsored by the Division of Carbohydrate Chemistry at the meeting of the American Chemical Society, New Orleans, Louisiana, August September 4, [N F Taylor; American Chemical Society.
Division of Carbohydrate Chemistry. In book: Fluorinated Heterocyclic Compounds: Synthesis, Chemistry, and Applications, pp - Cite this publication. the synthesis of fluorinated carbohydrates is. Protecting Group Manipulations in Carbohydrate Synthesis A. Lipta´k, A.
Borba´s, and I. Bajza, Carbohydrate Research Group of the Hungarian Academy of Sciences, neoglycopeptides), and their analogs.
Since carbohydrates are polyfunctional compounds, the chemical synthesis – even of the most simple derivatives – requires the File Size: KB. Galactose oxidase (GOase) was shown to oxidise several C2/C3 fluorinated galactose analogues. Interestingly, the enzyme was able to distinguish between the 2,3-tetrafluorinated galactose and its epimeric glucose analogue, and this represents.
A fluorine nuclear magnetic resonance (19F-NMR)-based method is employed to assess the binding preferences and interaction details of a library of synthetic fluorinated monosaccharides towards dendritic cell-specific intercellular adhesion molecule 3-grabbing non-integrin (DC-SIGN), a lectin of biomedical interest, which is involved in different viral infections, including HIV and Cited by: 4.
The rationale for designing fluorinated analogs of cell surface carbohydrates as anticancer agents is described. Using diethylaminosulfur trifluoride, a general and a convenient method for synthesis of 6-deoxyfluoro-hexosamines and 9-deoxyfluoro-N-acetylneuraminic acid has been reagent has also been used to introduce geminal fluorine both in the 6-position.
Edited by recognized experts, this book provides unique coverage of the wide-ranging uses and implications of fluorine and fluorinated compounds. Topics include medicinal monitoring and diagnosis, 19F MRI in medicine and in vivo cell tracking, 18F-labeled radiopharmaceuticals, brain imaging and neurology, risk assessment of reactive metabolites.
Purchase Advances in Carbohydrate Chemistry and Biochemistry, Volume 48 - 1st Edition. Print Book & E-Book. ISBNThe ¹H and ¹⁹F nuclear magnetic resonance (n.m.r.) spectra of a series of hexopyranosyl and pentopyranosyl fluorides were examined in some detail.
The ¹H n.m.r. analyses (first order) enabled the gross molecular conformations to be determined and at the same time provided an opportunity to check the anomeric assignments previously made through application of other. Agbanyo, M., and Taylor, N. F., Incorporation of 3-deoxyfluoro-D-glucose into glycogen and trehalose in fat body and flight muscle in Locusta migratoria, 6: – PubMed CrossRef Google ScholarAuthor: Kenneth L.
Kirk. Fluorine chemistry is an expanding area of research that is attracting international interest, due to the impact of fluorine in drug discovery and in clinical and molecular imaging (e.g. PET, MRI). Many researchers and academics are entering this area of research, while scientists in industrial and.
This book provides an overview of the impact that fluorine has made in the life sciences. In the first section, the emphasis is on how fluorine substitution of amino acids, peptides, nucleobases and carbohydrates can provide invaluable information at a molecular level.