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100   $a20180331g20129999  uy         0
101 0 $aeng
135   $aur|n|---|||||
181   $ctxt
182   $cc
183   $acr
200 00$aCarbohydrate chemistry $eproven synthetic methods /$fedited by Pavol Kovac
205   $a1st ed.
210  1$aBoca Raton, FL :$cCRC Press,$d2012-<2014->
215   $a1 online resource (318 p.)
225 1 $aCarbohydrate Chemistry
300   $aVol. 2 edited by: Gijsbert van der Marel, Jeroen Codee.
311 08$a1-4665-8357-6 
311 08$a1-4665-8358-4 
327   $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-?-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-?-d-gluco-heptopyranos-6-ulos-7-yl)phosphonate and Application for Carbon Chain Elongation""
327   $a""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-?-d-galactofuranosides (5-Deoxy-?-l-arabino-hexofuranosides) Starting from d-Galacturonic Acid Using Photoinduced Electron Transfer Deoxygenation""
327   $a""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-?-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""
327   $a""Chapter 24: Phenyl 2-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-?-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block""
330   $aFeaturing contributions from world-renowned experts and overseen by a highly respected series editor, Carbohydrate Chemistry: Proven Synthetic Methods, Volume 3 compiles reliable protocols for the preparation of intermediates for carbohydrate synthesis or other uses in the glycosciences. Exploring carbohydrate chemistry from both the academic and industrial points of view, this unique resource brings together useful information into one convenient reference. To ensure reproducibility, an independent checker has verified the experimental parts involved by repeating the protocols or using the methods.
410  0$aCarbohydrate Chemistry
606   $aCarbohydrates -- Synthesis
606   $aOrganic Chemistry$2HILCC
606   $aChemistry$2HILCC
606   $aPhysical Sciences & Mathematics$2HILCC
615  4$aCarbohydrates -- Synthesis.
615  7$aOrganic Chemistry
615  7$aChemistry
615  7$aPhysical Sciences & Mathematics
676   $a547.78
701   $aKova?c?$b Pavol$f1938-$01870606
801  0$bFlBoTFG
801  1$bFlBoTFG
906   $aBOOK
912   $a9910957519903321
996   $aCarbohydrate chemistry$94479123
997   $aUNINA