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Recent trends in carbohydrate chemis...
~
Somsak, Laszlo.
Recent trends in carbohydrate chemistrysynthesis, structure and function of carbohydrates /
Record Type:
Electronic resources : Monograph/item
Title/Author:
Recent trends in carbohydrate chemistryLaszlo 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.
Notes:
Acknowledgments
Online resource:
https://www.sciencedirect.com/science/book/9780128174678
ISBN:
9780128174685
Recent trends in carbohydrate chemistrysynthesis, structure and function of carbohydrates /
Somsak, Laszlo.
Recent trends in carbohydrate chemistry
synthesis, structure and function of carbohydrates /[electronic resource] :Laszlo Somsak ... [et al.]. - San Diego :Elsevier,2020. - 1 online resource (494 p.)
Description based upon print version of record.
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
ISBN: 9780128174685Index Terms--Genre/Form:
214472
Electronic books.
LC Class. No.: QD322.S95 / .R434 2020
Recent trends in carbohydrate chemistrysynthesis, structure and function of carbohydrates /
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synthesis, structure and function of carbohydrates /
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Laszlo Somsak ... [et al.].
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2020.
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Description based upon print version of record.
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Acknowledgments
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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
505
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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
505
8
$a
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
505
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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
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Electronic books.
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214472
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https://www.sciencedirect.com/science/book/9780128174678
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