Carbohydrate chemistry. Proven synthetic methods. Volume 3 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Roy, René (Editor ), Vidal, Sébastien (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Boca Raton, Florida ; London [England] ; New York : CRC Press, 2015.
Colección:Carbohydrate chemistry: proven synthetic methods ; Volume 3.
Temas:
Carbohydrates > Synthesis.
Organic Chemistry.
Chemistry.
Physical Sciences & Mathematics.
Glucides > Synthèse.
Carbohydrates > Synthesis
Acceso en línea:Texto completo
Tabla de Contenidos:
  • 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-Ü-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-Ü-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-Ý-d-galactofuranosides (5-Deoxy-Ü-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-Ü-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 13: Squaric Acid Diethyl Ester-Mediated Homodimerization of Unprotected Carbohydrates
  • Chapter 14: Thiol-Yne Coupling between Propargyl 2,3,4,6-Tetra-O-acetyl-Ý-d-glucopyranoside and Thiol : Expedient Access to Neoglycolipids.
  • Chapter 15: Lactose-Modified Triethoxysilane for the Surface Modification of Clay Nanocomposites
  • Chapter 16: Synthesis of 2-(Mannopyranosyloxy℗Ưmethyl) Benzo[b]furan through Sonogashira Coupling and Intramolecular Dehydrocyclization
  • Chapter 17: Stereocontrolled <U+00CC><U+0081>Y- and <U+00CC>˜U-Phosphorylations of d-Mannose
  • Chapter 18: Improved Synthesis of Ethyl 1-Thio-<U+00CC>˜U-d-galactofuranoside
  • Chapter 19: Improved Large-Scale Synthesis of <U+00CC><U+0081>Y-d-Arabinofuranose 1,2,5-Orthobenzoate
  • Chapter 20: Synthesis of Benzohydroxamic Acid Glucosides and Galactosides
  • Chapter 21: Hexa-O-benzoyl-4,6 -O-benzylidene- and p-Methoxybenzylidene-<U+00CC><U+0081>Y-lactose
  • Chapter 22: Conversion of Allyl 2-acetamido-2-deoxy-<U+00CC><U+0081>Y-d-glucopyranoside to Allyl 2-acetamido-2-deoxy-4,6-di-O-pivaloyl-<U+00CC><U+0081>Y-d-galactopyranoside
  • Chapter 23: Synthesis of 2,3:4,5-di-O-isopropylidene-d-Arabinose from d-Gluconolactone
  • Chapter 24: Phenyl 2-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-<U+00CC><U+0081>Y-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block
  • Chapter 25: Synthesis of Methyl 4-azido-2,3-di-O-benzoyl-4-deoxy-<U+00CC>˜U-l-arabino-pyranoside
  • Chapter 26: One-Pot Synthesis and Benzylation of Galactose, Glucose, and Mannose 1,2-Orthoesters
  • Chapter 27: 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-p-nitrophenoxycarbonyl-<U+00CC>˜U-d-glucopyranose
  • Chapter 28: Short Synthesis of (2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-<U+00CC><U+0081>Y-d-glucopyranosyl)benzene and 4-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-<U+00CC><U+0081>Y-d-glucopyranosyl)bromobenzene
  • Chapter 29: Isopropyl 2,3,4,6-Tetra-O-benzoyl-1-thio-<U+00CC><U+0081>Y-d-galactopyranoside, a Convenient Galactosyl Donor
  • Chapter 30: Facile Access to (1 3)-Glucosamine Linkages : Synthesis of Propyl 4,6-Di-O-benzyl-2-deoxy-2-trichloroacetamido-1-thio-<U+00CC><U+0081>Y-d-glucopyranoside
  • Chapter 31: Stereoselective Synthesis of 7-Deoxy-1,2
  • 3,4-di-O-isopropylidene-d-glycero-<U+00CC>˜U-d-galacto-heptopyranose.
  • Chapter 32: Synthesis of 4-Methoxyphenyl Ü-d-Rhamnopyranoside
  • Chapter 33: Synthesis of N-(4-Methoxybenzyl)-2-(Ü-d-glucopyranosyl)acetamide
  • Back Cover.

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