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Carbohydrate chemistry : proven synthetic methods / / edited by Pavol Kovac



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Titolo: Carbohydrate chemistry : proven synthetic methods / / edited by Pavol Kovac Visualizza cluster
Pubblicazione: Boca Raton, FL : , : CRC Press, , 2012- <2014->
Descrizione fisica: 1 online resource (318 p.)
Disciplina: 547.78
Soggetto topico: Carbohydrates -- Synthesis
Organic Chemistry
Chemistry
Physical Sciences & Mathematics
Altri autori: KovacPavol <1938->  
Note generali: Vol. 2 edited by: Gijsbert van der Marel, Jeroen Codee.
Nota di contenuto: ""Front Cover""; ""Contents""; ""Foreword""; ""Introduction""; ""Editors""; ""Series Editor""; ""Contributors""; ""Chapter 1: Synthesis of Higher-Carbon Sugars Using the Phosphonate Methodology : Part I-Synthesis of Methyl (methyl 2,3,4-Tri-O-benzyl-α-d-glucopyranosid)uronate""; ""Chapter 2: Synthesis of Higher-Carbon Sugars Using the Phosphonate Methodology : Part II-Synthesis of Dimethyl (methyl 2,3,4-Tri-O-benzyl-α-d-gluco-heptopyranos-6-ulos-7-yl)phosphonate and Application for Carbon Chain Elongation""
""Chapter 3: Preparation of Methyl, Butyl, Hexyl, and Octyl 2,3,4-Tri-O-acetyl-d-glucopyranuronates Using Microwave Irradiation""""Chapter 4: Metal-Free, Diamine-Mediated, Oxidative Monoamidation of Benzylated Carbohydrates""; ""Chapter 5: Metal-Free Oxidative Lactonization of Carbohydrates Using Molecular Iodine""; ""Chapter 6: Synthesis of Glycosyl Vinyl Sulfones for Bioconjugation""; ""Chapter 7: Synthesis of 5-Deoxy-β-d-galactofuranosides (5-Deoxy-α-l-arabino-hexofuranosides) Starting from d-Galacturonic Acid Using Photoinduced Electron Transfer Deoxygenation""
""Chapter 8: Glycal Transformation into 2-Deoxy Glycosides""""Chapter 9: Regioselective Preparation of 4-Deoxy-erythro-hex-4-enopyranoside Enol Ethers through Acetone Elimination""; ""Chapter 10: Stereoselective Reduction Using Sodium Triacetoxyborodeuteride : Synthesis of Methyl 2,3-Di-O-benzyl-α-d-(4-2H)-glucopyranoside""; ""Chapter 11: Selective Anomeric S-Deacetylation Using Aqueous Sodium Methanethiolate""; ""Chapter 12: Glycosylation of Phenolic Acceptors Using Benzoylated Glycosyl Trichloroacetimidate Donors""
""Chapter 24: Phenyl 2-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-β-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block""
Titolo autorizzato: Carbohydrate chemistry  Visualizza cluster
ISBN: 1-4987-6018-X
0-429-10242-9
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910788108103321
Lo trovi qui: Univ. Federico II
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Serie: Carbohydrate Chemistry