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Recent trends in carbohydrate chemis...
Somsak, Laszlo.

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  • Recent trends in carbohydrate chemistry = synthesis, structure and function of carbohydrates /
  • Record Type: Electronic resources : Monograph/item
    Title/Author: Recent trends in carbohydrate chemistry/ Laszlo Somsak ... [et al.].
    Reminder of title: synthesis, structure and function of carbohydrates /
    Author: Somsak, Laszlo.
    Published: San Diego :Elsevier, : 2020.,
    Description: 1 online resource (494 p.)
    Notes: Description based upon print version of record.
    [NT 15003449]: Intro -- Recent Trends in Carbohydrate Chemistry: Synthesis, Structure and Function of Carbohydrates -- Copyright -- Contents -- Contributors -- Preface -- Part One: Monosaccharide chemistry toward molecular diversity-Recent findings -- 1: Perspective on the transformation of carbohydrates under green and sustainable reaction conditions -- 1 Introduction -- 2 Synthetic transformations of carbohydrates using nonhazardous environmentally benign solvents -- 3 Transformations of carbohydrates in water -- 4 Transformations of carbohydrates in room temperature ionic liquids
    [NT 15003449]: 5 Use of ionic liquids as reaction solvents -- 6 Ionic liquid tags in enzymatic reactions -- 7 Transformation of carbohydrates in supercritical fluids -- 8 Transformation of carbohydrates in deep eutectic solvents -- 9 Transformation of carbohydrates using fluorous solvents -- 10 Transformation of carbohydrates using nonconventional energy sources -- 11 Oligosaccharide synthesis using microwave irradiation -- 12 Transformation of carbohydrates using ball milling -- 13 Sonication-assisted transformations of carbohydrates -- 14 Ultrasound-mediated functionalization of carbohydrates
    [NT 15003449]: 4 A 3 -coupling of bio-based furanic aldehydes -- 5 Ugi-type reactions -- 6 Kabachnik-Fields reaction -- 7 Multicomponent dipolar cycloadditions -- 8 Conclusion -- Acknowledgments -- References -- 3: Alkyne dicobalt complexes in carbohydrates: Synthetic applications -- 1 Introduction -- 2 Dicobalt hexacarbonyl-mediated anomerization of alkynyl C-glycosides -- 3 Dicobalt hexacarbonyl-mediated ring-opening of alkynyl C-glycosides -- 4 Dicobalt hexacarbonyl-mediated formation of ether rings from sugar acetylenes -- 5 Glycosylations based on alkyne dicobalt hexacarbonyl complexes
    [NT 15003449]: 6 Dicobalt hexacarbonyl-mediated Ferrier(II)-type carbocyclizations from pyranose derivatives -- 7 Pyranosidic dicobalt hexacarbonyl propargyl oxycarbenium ions versus oxycarbenium ions-Some remarkable features -- 8 Dicobalt hexacarbonyl complexes of alkynyl compounds as precursors of pyranosidic Ferrier-Nicholas cations-Synthesi ... -- 8.1 Ferrier rearrangement or Ferrier(I) reaction-Ferrier- Nicholas cations -- 8.2 C1-Ferrier-Nicholas cations -- 8.3 C3-Ferrier-Nicholas cations -- 8.4 Ferrier-Nicholas systems based on (2-deoxy-2-C-methylenepyranosyl)alkynes -- 9 Conclusion
    Online resource: https://www.sciencedirect.com/science/book/9780128174678
    ISBN: 9780128174685
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W9406982 電子資源 11.線上閱覽_V 電子書 EB QD322.S95 .R434 2020 一般使用(Normal) On shelf 0
  • 1 records • Pages 1 •
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