008 |
|
200509s2020 cau o ||| 0 eng d |
020 |
|
|a9780128174685
|
020 |
|
|a0128174684
|
040 |
|
|aEBLCP|beng|cEBLCP
|
041 |
0
|
|aeng
|
050 |
4
|
|aQD322.S95|b.R434 2020
|
095 |
|
|aNF|tLCC|p|dQD322.S95|e|c
|
100 |
1
|
|aSomsak, Laszlo.
|
245 |
10
|
|aRecent trends in carbohydrate chemistry|h[electronic resource] :|bsynthesis, structure and function of carbohydrates /|cLaszlo Somsak ... [et al.].
|
260 |
|
|aSan Diego :|bElsevier,|c2020.
|
300 |
|
|a1 online resource (494 p.)
|
500 |
|
|aDescription based upon print version of record.
|
500 |
|
|aAcknowledgments
|
505 |
0
|
|aIntro -- 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 |
8
|
|a5 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
|
|a4 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 |
8
|
|a6 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
|
655 |
0
|
|aElectronic books.
|
856 |
40
|
|uhttps://www.sciencedirect.com/science/book/9780128174678
|