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[null,"1.","Record Nr.",null,"UNINA9910788108103321"]
[null,null,"Titolo",null,"Carbohydrate chemistry : proven synthetic methods / / edited by Pavol Kovac"]
[null,null,"Pubbl/distr/stampa",null,"Boca Raton, FL : , : CRC Press, , 2012- <2014->"]
[null,null,"ISBN",null,"1-4987-6018-X"]
[{"$nulls":4},"0-429-10242-9"]
[null,null,"Descrizione fisica",null,"1 online resource (318 p.)"]
[null,null,"Collana",null,"Carbohydrate Chemistry"]
[null,null,"Disciplina",null,"547.78"]
[null,null,"Soggetti",null,"Carbohydrates -- Synthesis"]
[{"$nulls":4},"Organic Chemistry"]
[{"$nulls":4},"Chemistry"]
[{"$nulls":4},"Physical Sciences & Mathematics"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Vol. 2 edited by: Gijsbert van der Marel, Jeroen Codee."]
[null,null,"Nota di contenuto",null,"\"\"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\"\""]
[{"$nulls":4},"\"\"Chapter 3: Preparation of Methyl, Butyl, Hexyl, and Octyl 2,3,4-Tri-O-acetyl-d-glucopyranuronates Using Microwave Irradiation\"\"\"\"Chapter 4: Metal-Free, Diamine-Mediated, Oxidative Monoamidation of Benzylated Carbohydrates\"\"; \"\"Chapter 5: Metal-Free Oxidative Lactonization of Carbohydrates Using Molecular Iodine\"\"; \"\"Chapter 6: Synthesis of Glycosyl Vinyl Sulfones for Bioconjugation\"\"; \"\"Chapter 7: Synthesis of 5-Deoxy-β-d-galactofuranosides (5-Deoxy-α-l-arabino-hexofuranosides) Starting from d-Galacturonic Acid Using Photoinduced Electron Transfer Deoxygenation\"\""]
[{"$nulls":4},"\"\"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\"\"; "]
[{"$nulls":4},"\"\"Chapter 11: Selective Anomeric S-Deacetylation Using Aqueous Sodium Methanethiolate\"\"; \"\"Chapter 12: Glycosylation of Phenolic Acceptors Using Benzoylated Glycosyl Trichloroacetimidate Donors\"\""]
[{"$nulls":4},"\"\"Chapter 24: Phenyl 2-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-β-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block\"\""]