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| 245 |
0 |
0 |
|a Carbohydrate chemistry.
|p Proven synthetic methods.
|n Volume 3 /
|c edited by René Roy Sébastien Vidal.
|
| 264 |
|
1 |
|a Boca Raton, Florida ;
|a London [England] ;
|a New York :
|b CRC Press,
|c 2015.
|
| 264 |
|
4 |
|c ©2015
|
| 300 |
|
|
|a 1 online resource (318 pages) :
|b illustrations, tables
|
| 336 |
|
|
|a text
|b txt
|2 rdacontent
|
| 337 |
|
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|a computer
|b c
|2 rdamedia
|
| 338 |
|
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|a online resource
|b cr
|2 rdacarrier
|
| 490 |
1 |
|
|a Carbohydrate Chemistry : Proven Synthetic Methods ;
|v Volume 3
|
| 504 |
|
|
|a Includes bibliographical references at the end of each chapters.
|
| 588 |
0 |
|
|a Online resource; title from PDF title page (ebrary, viewed June 15, 2015).
|
| 505 |
0 |
|
|a 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.
|
| 505 |
8 |
|
|a 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.
|
| 505 |
8 |
|
|a Chapter 32: Synthesis of 4-Methoxyphenyl Ü-d-Rhamnopyranoside -- Chapter 33: Synthesis of N-(4-Methoxybenzyl)-2-(Ü-d-glucopyranosyl)acetamide -- Back Cover.
|
| 546 |
|
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|a English.
|
| 590 |
|
|
|a ProQuest Ebook Central
|b Ebook Central Academic Complete
|
| 650 |
|
0 |
|a Carbohydrates
|x Synthesis.
|
| 650 |
|
4 |
|a Organic Chemistry.
|
| 650 |
|
4 |
|a Chemistry.
|
| 650 |
|
4 |
|a Physical Sciences & Mathematics.
|
| 650 |
|
6 |
|a Glucides
|x Synthèse.
|
| 650 |
|
7 |
|a Carbohydrates
|x Synthesis
|2 fast
|
| 700 |
1 |
|
|a Roy, René,
|e editor.
|
| 700 |
1 |
|
|a Vidal, Sébastien,
|e editor.
|
| 758 |
|
|
|i has work:
|a Volume 3 Proven synthetic methods Carbohydrate chemistry (Text)
|1 https://id.oclc.org/worldcat/entity/E39PCG8xDvFhjckMQFKWkTwFjy
|4 https://id.oclc.org/worldcat/ontology/hasWork
|
| 776 |
0 |
8 |
|i Print version:
|t Carbohydrate chemistry. Proven synthetic methods. Volume 3.
|d Boca Raton, Florida ; London, [England] ; New York : CRC Press, ©2015
|h xlvii, 266 pages
|k Carbohydrate Chemistry : Proven Synthetic Methods ; Volume 3
|z 9781466583573
|
| 830 |
|
0 |
|a Carbohydrate chemistry: proven synthetic methods ;
|v Volume 3.
|
| 856 |
4 |
0 |
|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=3563635
|z Texto completo
|
| 880 |
8 |
|
|6 505-00/(S
|a 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 -β-- and α-Phosphorylations of d-Mannose -- Chapter 18: Improved Synthesis of Ethyl 1-Thio-α-d-galactofuranoside -- Chapter 19: Improved Large-Scale Synthesis of -β--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-β-lactose -- Chapter 22: Conversion of Allyl 2-acetamido-2-deoxy-β-d-glucopyranoside to Allyl 2-acetamido-2-deoxy-4,6-di-O-pivaloyl-β-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-β-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block -- Chapter 25: Synthesis of Methyl 4-azido-2,3-di-O-benzoyl-4-deoxy-α-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-α-d-glucopyranose -- Chapter 28: Short Synthesis of (2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-d-glucopyranosyl)benzene and 4-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-d-glucopyranosyl)bromobenzene -- Chapter 29: Isopropyl 2,3,4,6-Tetra-O-benzoyl-1-thio-β-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-β-d-glucopyranoside -- Chapter 31: Stereoselective Synthesis of 7-Deoxy-1,2 -- 3,4-di-O-isopropylidene-d-glycero-α-d-galacto-heptopyranose.
|
| 880 |
8 |
|
|6 505-00/(S
|a Chapter 32: Synthesis of 4-Methoxyphenyl α-d-Rhamnopyranoside -- Chapter 33: Synthesis of N-(4-Methoxybenzyl)-2-(α-d-glucopyranosyl)acetamide -- Back Cover.
|
| 880 |
0 |
|
|6 505-00/(S
|a 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 13: Squaric Acid Diethyl Ester-Mediated Homodimerization of Unprotected Carbohydrates -- Chapter 14: Thiol-Yne Coupling between Propargyl 2,3,4,6-Tetra-O-acetyl-β-d-glucopyranoside and Thiol : Expedient Access to Neoglycolipids.
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