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Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides


Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides


1. Aufl.

von: Biao Yu, Xiaoyu Yang

124,99 €

Verlag: Wiley-VCH (D)
Format: EPUB
Veröffentl.: 20.03.2024
ISBN/EAN: 9783527817900
Sprache: englisch
Anzahl Seiten: 304

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Beschreibungen

<b>Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides</b> <p> <b>Revolutionize your manufacturing processes and more with this groundbreaking introduction</b> <p>Carbohydrates and complex glycosides are important classes of molecules. The ubiquitous glycosides are extremely diverse in structure and functions, and many of them are of pharmacological significance. Purification of a homogeneous glycoside from the nature sources, especially in an appreciable amount, is always difficult. Chemical synthesis provides a feasible access to the homogenous glycosides and their congeners. <p><i>Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides </i>presents about 10 families of naturally occurring glycoside natural products, including about 150 molecules that organic chemists have devoted a lot of effort toward their synthesis. In each example, the background of each natural glycoside, including its natural resources, its isolation process and its bioactivities have been described; the total synthesis of the natural glycoside is presented with special emphasis on the glycosylation reaction, the strategy on saccharides assembly, the protecting group manipulation, and the method for the synthesis of the rare saccharide units. Readers can clearly see the progress of total synthesis of naturally occurring glycosides, from early to current arts, from simple to complex molecules, and from tedious strategy to highly efficient and economical methodologies in this book. It will highly benefit the further developments in the total synthesis of naturally occurring glycosides and synthetic carbohydrate chemistry. <p><i>Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides </i>is ideal for Organic Chemists, Biochemists, Pharmaceutical and Medicinal Chemists, Natural Products Chemists, and Pharmaceutical Industry
<p>Preface xi</p> <p>List of Abbreviations xiii</p> <p><b>1 Introduction 1</b></p> <p>References 5</p> <p><b>2 Aromatic Polyketide Glycosides 7</b></p> <p>Landomycin A 7</p> <p>Olivomycin A 13</p> <p>Ciclamycin 17</p> <p>Vineomycin B2 20</p> <p>Trioxacarcin 25</p> <p>Daunorubicin 29</p> <p>Aquayamycin 30</p> <p>Vineomycin A1 30</p> <p>Derhodinosylurdamycin A 31</p> <p>Jadomycins 31</p> <p>Tan-1085 33</p> <p>Benanomicins and Pradimicins 33</p> <p>Pluramycins 34</p> <p>Marmycins 35</p> <p>Cassialoin 36</p> <p>FD-594 36</p> <p>Calixanthomycin A 38</p> <p>Lactonamycin 38</p> <p>Lomaiviticin A(−) 39</p> <p>References 42</p> <p><b>3 Enediyne Glycosides 47</b></p> <p>Calicheamicin γ<sub>I</sub><sup>1</sup> 48</p> <p>Namenamicin 54</p> <p>Shishijimicin A 56</p> <p>Neocarzinostatin Chromophore 58</p> <p>Maduropeptin Chromophore 59</p> <p>References 61</p> <p><b>4 Flavonoid Glycosides 63</b></p> <p>Flavonol 3-O-glycosides 65</p> <p>Quercetin 3-sophorotrioside 65</p> <p>Sl0101 66</p> <p>Flavone and Isoflavone 7-O-Glycosides 67</p> <p>A-76202 67</p> <p>Flavonol 3-O- and 7-O-Bisglycosides 70</p> <p>Kaempferitrin 70</p> <p>Flavonol 5-O-Glycosides 71</p> <p>Camellianin B 71</p> <p>Flavone 6-C-Glycosides 72</p> <p>Chafurosides 72</p> <p>Cyanidin 3-O-Glycosides 74</p> <p>Cyanidin 3-O-β-D-glucoside 74</p> <p>Other Examples 75</p> <p>Quercetin 3-O-β-D-Glucuronide 75</p> <p>Quercetin 3-O-(2 ′′-Galloyl)-α-L-arabinopyranoside 75</p> <p>Isoquercitrin Coumarate 75</p> <p>Kaempferol 3-O-(3 ′′,6′′-di-O-E-p-coumaroyl)-β-D-Glucopyranoside 76</p> <p>Platanoside 76</p> <p>Quercetin-3-O-trisaccharide 79 78</p> <p>Houttuynoid A 78</p> <p>Daidzin, Genistin, Ononin, and Sissotrin 78</p> <p>Apigenin 7-O-Cellobioside 79</p> <p>Suttellarin 80</p> <p>Calabricoside A 80</p> <p>Kaempferol-3-O-7-O-bisglycoside 88 81</p> <p>Vicenines 81</p> <p>Carambolaflavone A 83</p> <p>Flavocommeline 83</p> <p>Schaftoside 84</p> <p>Pelargonidin 3-O-6′′-O-acetyl-β-D-glucopyranoside 85</p> <p>Cyanidin 4′-O-methyl-3-O-glucoside 86</p> <p>References 86</p> <p><b>5 Macrolide Glycosides 89</b></p> <p>Erythromycin 89</p> <p>Apoptolidin A 94</p> <p>Spinosyn A (Lepicidin A) 98</p> <p>Tiacumicin B 103</p> <p>Pikromycin 106</p> <p>Polycavernoside A 106</p> <p>Auriside A 107</p> <p>Lyngbyaloside B 108</p> <p>Avermectin 109</p> <p>Formamicin 109</p> <p>Tylosin 109</p> <p>Mangrolide 112</p> <p>Amphotericin B 113</p> <p>Aldgamycins 113</p> <p>Mycinamicin IV 114</p> <p>References 115</p> <p><b>6 Nucleosides 119</b></p> <p>Tunicamycin 119</p> <p>Hikizimycin 126</p> <p>Herbicidins 128</p> <p>A201A 131</p> <p>Amipurimycin 134</p> <p>Caprazamycin 137</p> <p>Polyoxin J 141</p> <p>Octosyl Acid A 142</p> <p>HF-7 143</p> <p>Malayamycin 143</p> <p>Capuramycin 144</p> <p>Muraymycin 144</p> <p>Plicacetin, Streptcytosine A, and Amicetin 145</p> <p>A-94964 146</p> <p>Miharamycin B 148</p> <p>References 149</p> <p><b>7 Peptide Glycosides 153</b></p> <p>Vancomycin 155</p> <p>Bleomycin A2 159</p> <p>Mannopeptimycin 165</p> <p>Syndecan 170</p> <p>Lipoglycopeptide Arylomycin 171</p> <p>References 172</p> <p><b>8 Resin Glycosides 175</b></p> <p>Calonyctin A 176</p> <p>Tricolorin 179</p> <p>Ipomoeassin 185</p> <p>Woodrosin I 189</p> <p>Batatosides l 191</p> <p>Batatin VI 191</p> <p>Merremoside d 192</p> <p>Murucoidins 192</p> <p>References 195</p> <p><b>9 Steroid Glycosides 197</b></p> <p>Cholestane Type Steroid Glycosides 197</p> <p>OSW-1 197</p> <p>Periploside A 201</p> <p>Luzonicosides and Sepositoside 204</p> <p>Cardenolide Type Steroid Glycosides 207</p> <p>Digitoxin 207</p> <p>Furostane Type Steroid Glycosides 212</p> <p>Furostan Saponin and Methyl Protodioscin 212</p> <p>Spirostan Type Steroid Glycosides 214</p> <p>Desgalactotigonin 214</p> <p>Forbeside E 216</p> <p>Osladin 216</p> <p>Pavonimin 218</p> <p>Dioscin 218</p> <p>Polyphyllin D 219</p> <p>Maidong Saponin C 220</p> <p>Xiebai Saponin I 221</p> <p>Candicanoside A 222</p> <p>Ouabain 222</p> <p>Timosaponin BII 223</p> <p>Solamargine 223</p> <p>Rhodexins 225</p> <p>Goniopectenoside B 226</p> <p>Astrosterioside A 226</p> <p>Linckoside 227</p> <p>Trewianin 228</p> <p>P57 228</p> <p>Oleandrin 230</p> <p>References 231</p> <p><b>10 Triterpenoid Glycosides 233</b></p> <p>Ciwujianoside C3 233</p> <p>QS-21 234</p> <p>Lobatoside E 238</p> <p>Ginsenosides 239</p> <p>Echinoside A 242</p> <p>Anemoclemoside B 245</p> <p>Betavugaroside III 247</p> <p>Δ<sup>20</sup>-Ginsenosides 247</p> <p>Flaccidoside II 248</p> <p>Asiaticoside 249</p> <p>Pulsatilla Saponin D 249</p> <p>Lotoidoside D 250</p> <p>Astragalosides 252</p> <p>Chikusetsu Saponins 253</p> <p>References 253</p> <p><b>11 Miscellaneous Glycosides 257</b></p> <p>Allosamidin 257</p> <p>Staurosporine 257</p> <p>Everninomicin 13,384-1 259</p> <p>Brasilicardins 263</p> <p>Efrotomycin 266</p> <p>Peyssonoside A 267</p> <p>Amycolamicin/Kibdelomycin 268</p> <p>Strictosidine-Type Indole Alkaloid Glycosides 268</p> <p>Cotylenin A 270</p> <p>Pyrolaside B 271</p> <p>References 273</p> <p>Index 275</p>
<p><i><b>Biao Yu </b>is Professor and currently Director of State Key Laboratory of Bioorganic and Natural Products Chemistry at Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences. He was given the Humboldt Research Award from the Alexander von Humboldt Foundation in 2020, the Roy L. Whistler Award from the International Carbohydrate Organization in 2022, and was elected as the Academician of the Chinese Academy of Sciences in 2021. He has spent nearly 30 years working on carbohydrate chemistry, especially the total synthesis of naturally occurring glycosides. </i> <p><i><b>Xiaoyu Yang </b>is Associate Professor at the School of Physical Science and Technology, ShanghaiTech University, China. His research interests focus on organic synthesis, asymmetric catalysis, carbohydrate chemistry and chemical biology.</i>
<p> <b>Revolutionize your manufacturing processes and more with this groundbreaking introduction</b> <p>Carbohydrates and complex glycosides are important classes of molecules. The ubiquitous glycosides are extremely diverse in structure and functions, and many of them are of pharmacological significance. Purification of a homogeneous glycoside from the nature sources, especially in an appreciable amount, is always difficult. Chemical synthesis provides a feasible access to the homogenous glycosides and their congeners. <p><i>Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides </i>presents about 10 families of naturally occurring glycoside natural products, including about 150 molecules that organic chemists have devoted a lot of effort toward their synthesis. In each example, the background of each natural glycoside, including its natural resources, its isolation process and its bioactivities have been described; the total synthesis of the natural glycoside is presented with special emphasis on the glycosylation reaction, the strategy on saccharides assembly, the protecting group manipulation, and the method for the synthesis of the rare saccharide units. Readers can clearly see the progress of total synthesis of naturally occurring glycosides, from early to current arts, from simple to complex molecules, and from tedious strategy to highly efficient and economical methodologies in this book. It will highly benefit the further developments in the total synthesis of naturally occurring glycosides and synthetic carbohydrate chemistry. <p><i>Carbohydrate Chemistry in the Total Synthesis of Naturally Occurring Glycosides </i>is ideal for Organic Chemists, Biochemists, Pharmaceutical and Medicinal Chemists, Natural Products Chemists, and Pharmaceutical Industry

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