Glycoscience: Chemistry and Chemical Biology I–III

Glycoscience has become a term covering all sorts of activities and applications within or at the edge of carbohydrate research. Glycostructures play a highly diverse and crucial role in a myriad of organisms and important systems in biology, physiology, medicine, bioengineering and technology. Only...

Full description

Bibliographic Details
Other Authors: Fraser-Reid, Bertram O. (Editor), Tatsuta, Kuniaki (Editor), Thiem, Joachim (Editor)
Format: eBook
Language:English
Published: Berlin, Heidelberg Springer Berlin Heidelberg 2001, 2001
Edition:1st ed. 2001
Subjects:
Online Access:
Collection: Springer Book Archives -2004 - Collection details see MPG.ReNa
LEADER 06335nmm a2200445 u 4500
001 EB000665240
003 EBX01000000000000000518322
005 00000000000000.0
007 cr|||||||||||||||||||||
008 140122 ||| eng
020 |a 9783642568749 
100 1 |a Fraser-Reid, Bertram O.  |e [editor] 
245 0 0 |a Glycoscience: Chemistry and Chemical Biology I–III  |h Elektronische Ressource  |c edited by Bertram O. Fraser-Reid, Kuniaki Tatsuta, Joachim Thiem 
246 3 1 |a with contributions by numerous experts 
250 |a 1st ed. 2001 
260 |a Berlin, Heidelberg  |b Springer Berlin Heidelberg  |c 2001, 2001 
300 |a CXX, 2872 p. 78 illus  |b online resource 
505 0 |a Volume I -- 1 General Principles -- 1.1 Structure and Conformation of Carbohydrates -- 1.2 Properties of Carbohydrates -- 1.3 Separation and Purification of Carbohydrates -- 1.4 General Occurrence of Carbohydrates -- 2 General Synthetic Methods: Reactions at Non Anomeric Positions -- 2.1 Reactions at Oxygen Atoms -- 2.2 Oxidation and Reduction -- 2.3 Deoxygenation -- 2.4 Heteroatom Exchange -- 2.5 Anhydrosugars -- 2.6 C-C Bond Formation -- 2.7 C=C Bond Formation -- 2.8 Degradation Reactions -- 2.9 Rearrangement Reactions -- 3 General Synthetic Methods: Reactions at the Anomeric Center -- 3.1 Reactions at Oxygen Atoms -- 3.2 Oxidation, Reduction and Deoxygenation -- 3.3 Heteroatom Exchange: Glycosylation -- 3.3.1 Mechanistic Aspects -- 3.3.2 Glycosides as Donors -- 3.3.3 Glycosyl Halides and Anomeric Esters as Donors -- 3.4 Anomeric Anhydro Sugars -- 3.5 S-Glycosylation -- 3.6 N-Glycosylation -- 3.7 C-Glycosylation -- 3.8 Formation and Reactions of Glycal Derivatives --  
505 0 |a 10 Glycomimetics -- 10.1 Introduction -- 10.2 Azaglycomimetics: Synthesis and Chemical Biology -- 10.3 Carbasugars: Synthesis and Functions -- 10.4 Sulfur Containing Glycomimetics -- 10.5 C-Glycosyl Analogs of Oligosaccharides and Glycosyl Amino Acids -- 10.6 Non-Sugar Glycomimetics -- IUPAC’s 1996 Recommendations on Nomenclature of Carbohydrates 
505 0 |a 5.5.3 Multivalency in Protein-Carbohydrate Recognition -- Volume III -- 6 Complex Polysaccharides -- 6.1 Occurrence and Significance -- 6.2 Properties -- 6.3 Synthesis of Sulfated Glycosaminoglycans -- 6.4 Biosynthesis and Degradation -- 6.5 Chemical Biology and Biomedicine -- 6.5.1 General Aspects -- 6.5.2 Mycobacterial Cell Wall Components -- 7 Glycolipids -- 7.1 Occurrence and Significance -- 7.2 Properties -- 7.3 Synthesis -- 7.4 Biosynthesis and Degradation -- 7.5 Chemical Biology and Biomedicine: Glycolipids and Glycosphingolipids -- 8 Glycoproteins -- 8.1 Occurrence and Significance -- 8.2 Properties -- 8.3 Synthesis and Applications of Biologically Relevant Glycopeptides -- 8.4 Chemical Biology and Biomedicine: Enkephalin-Derived Glycopeptide Analgesics -- 9 Other Glycoconjugates -- 9.1 Antitumor and Antimicrobial Glycoconjugates -- 9.2 Synthesis of Enediyne Antibiotic Oligosaccharides -- 9.3 Chemical Biology and Biomedicine of Glycosylated Natural Compounds --  
505 0 |a 3.9 Degradation and Rearrangement Reactions -- Volume II -- 4 Monosaccharides -- 4.1 Occurrence and Significance -- 4.2 Properties -- 4.3 Synthesis of Biologically Relevant Monosaccharides -- 4.4 De Novo Synthesis of Monosaccharides -- 4.5 Formation of Complex Natural Compounds from Monosaccharides -- 4.6 Biosynthesis and Degradation -- 4.7 Chemical Biology and Biomedicine -- 5 Oligosaccharides -- 5.1 Occurrence and Significance -- 5.2 Properties -- 5.3 Synthesis -- 5.3.1 Enzymatic Glycosylation -- 5.3.2 Glycosyl Halides in Oligosaccharide Synthesis -- 5.3.3 Regio-and Stereoselective Methods of Glycosylation -- 5.3.4 Stereoselective Synthesis of ß-manno Glycosides -- 5.3.5 Combinatorial and Solid Phase Methods in Oligosaccharide Synthesis -- 5.4 Biosynthesis and Degradation of Galactosyloligosaccharides .... -- 5.5 Chemical Biology and Biomedicine -- 5.5.1 Glycosylphosphatidylinositols -- 5.5.2 Mammalian Carbohydrate-Lectin Interactions --  
653 |a Molecular Medicine 
653 |a Molecular biology 
653 |a Food—Biotechnology 
653 |a Food Science 
653 |a Biochemistry, general 
653 |a Biotechnology 
653 |a Organic Chemistry 
653 |a Organic chemistry 
653 |a Biotechnology 
653 |a Biochemistry 
653 |a Pharmacology 
653 |a Pharmacology/Toxicology 
700 1 |a Tatsuta, Kuniaki  |e [editor] 
700 1 |a Thiem, Joachim  |e [editor] 
041 0 7 |a eng  |2 ISO 639-2 
989 |b SBA  |a Springer Book Archives -2004 
856 4 0 |u https://doi.org/10.1007/978-3-642-56874-9?nosfx=y  |x Verlag  |3 Volltext 
082 0 |a 547 
520 |a Glycoscience has become a term covering all sorts of activities and applications within or at the edge of carbohydrate research. Glycostructures play a highly diverse and crucial role in a myriad of organisms and important systems in biology, physiology, medicine, bioengineering and technology. Only in recent years have the tools been developed to partly understand the highly complex functions and the chemistry behind them, but many facts still remain undiscovered. "All roads lead to carbohydrates ... we cannot do without them." (K.C. Nicolaou). Presently the field is experiencing a "quantum jump". Therefore the editors have drawn together in this three volume set plus an accompanying CD-ROM, the complete and up-to-date information on glycostructures, their chemistry and chemical biology, and present them in the form of a comprehensive and strictly systematic survey. Methodology oriented introductory chapters are followed by a homogeneous and systematic approach (occurrence, properties, synthesis, biosynthesis and degradation, chemical biology and medicine) arranged according to classes of glycostructures. The texts are furnished by 2.670 figures, chemical structures and reaction schemes (including more than 12.000 individual chemical reactions), and more than 9.000 references. The stimulating and readily accessible volumes of Glycoscience - Chemistry and Chemical Biology have been designed as the essential resource for both the experts in the field and the large community of investigators in fields like biomedicine, cancer research, pharmaceutical and biochemistry, biology, food science, agriculture or (bio-)engineering