LEADER 03488oam 2200613I 450 001 9910788108103321 005 20230801231935.0 010 $a1-4987-6018-X 010 $a0-429-10242-9 024 7 $a10.1201/b18400 035 $a(CKB)2670000000618223 035 $a(EBL)3563635 035 $a(SSID)ssj0001542491 035 $a(PQKBManifestationID)16131944 035 $a(PQKBTitleCode)TC0001542491 035 $a(PQKBWorkID)14791919 035 $a(PQKB)11012314 035 $a(MiAaPQ)EBC3563635 035 $a(OCoLC)911047754 035 $a(EXLCZ)992670000000618223 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 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 $a1-4665-8357-6 311 $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 $a""Chapter 24: Phenyl 2-O-acetyl-3-O-allyl-4-O-benzyl-1-thio-?-d-glucopyranoside, a Versatile, Orthogonally Protected Building Block"" 410 0$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 $aKovac$b Pavol$f1938-$01531526 801 0$bFlBoTFG 801 1$bFlBoTFG 906 $aBOOK 912 $a9910788108103321 996 $aCarbohydrate chemistry$93777260 997 $aUNINA