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Titlebook: Glycoscience; Synthesis of Oligosa Hugues Driguez,Joachim Thiem Book 1997 Springer-Verlag Berlin Heidelberg 1997 Alkaloid.carbohydrates.cat

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書目名稱Glycoscience
副標(biāo)題Synthesis of Oligosa
編輯Hugues Driguez,Joachim Thiem
視頻videohttp://file.papertrans.cn/388/387107/387107.mp4
概述Very affordable price *.For the personal libraries of graduates and scientists working at the cutting edge of academic, industrial and pharmaceutical research.
叢書名稱Springer Desktop Editions in Chemistry
圖書封面Titlebook: Glycoscience; Synthesis of Oligosa Hugues Driguez,Joachim Thiem Book 1997 Springer-Verlag Berlin Heidelberg 1997 Alkaloid.carbohydrates.cat
描述This book presents the state of the art in the synthesis very complex saccharide structures, written by leading scientists at the forefront of this rapidly growing field. Reflecting the particular significance in recent years of efficient and selective procedures employing enzymes for preparative purposes in the carbohydrate field, a major proportion of the articles focus on these biocatalytic methods. In addition, recent strategies for the construction of unusual carbohydrates structures employing novel and creative methodologies are highlighted. Further, particular emphasis is placed on very complex saccharide structures as well as on special solutions to problems that are particularly challenging.
出版日期Book 1997
關(guān)鍵詞Alkaloid; carbohydrates; catalysis; enzyme; enzymes; Oligosaccharid; Peptid; synthesis
版次1
doihttps://doi.org/10.1007/BFb0119216
isbn_softcover978-3-540-65557-2
isbn_ebook978-3-540-49629-8
copyrightSpringer-Verlag Berlin Heidelberg 1997
The information of publication is updating

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Synthesis of oligosaccharides of bacterial origin containing heptoses, uronic acids and fructofuran excellent yields of α-linked fructofuranosyl disaccharides are obtained. Application of the internal aglycon delivery approach, with the aglycon tethered to the .-face of the fructofuranosyl thioglycoside donor as part of a 3-.-.-methoxybenzylidene acetal, produced stereospecifically high yields of
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,Die Eiwei?fasern (Proteinfasern),ialic acids. This review examines the most recent methods used for the synthesis and modification of sialic acids and for the preparation of sialyl glycosides as biological probes of sialic acid-recognising proteins.
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Erratum to: Telephonie und Mikrophonie,que and structurally complex carbohydrate-related compounds that may be regarded as metabolically stable mimetics of oligosaccharides and that are thus of interest because of their potential bioactivity.
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Tandem asymmetric C-C bond formations by enzyme catalysis,que and structurally complex carbohydrate-related compounds that may be regarded as metabolically stable mimetics of oligosaccharides and that are thus of interest because of their potential bioactivity.
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https://doi.org/10.1007/978-3-662-41113-1d when looking for a given selectivity. Some selected examples of diand oligosaccharide synthesis by glycosidase-catalyzed reactions are included to illustrate the scope of this methodology. The use of lipases in organic solvents for acylation and deacylation reactions of carbohydrates is also described in some detail.
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