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Recent trends in carbohydrate chemis...

Somsak, Laszlo.

Recent trends in carbohydrate chemistrysynthesis, structure and function of carbohydrates /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Recent trends in carbohydrate chemistryLaszlo Somsak ... [et al.].
其他題名:	synthesis, structure and function of carbohydrates /
作者:	Somsak, Laszlo.
出版者:	San Diego :Elsevier,2020.
面頁冊數:	1 online resource (494 p.)
附註:	Description based upon print version of record.
附註:	Acknowledgments
電子資源:	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 chemistrysynthesis, 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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245 1 0 $a Recent trends in carbohydrate chemistry $h [electronic resource] : $b synthesis, structure and function of carbohydrates / $c Laszlo Somsak ... [et al.].
260 $a San Diego : $b Elsevier, $c 2020.
300 $a 1 online resource (494 p.)
500 $a Description based upon print version of record.
500 $a Acknowledgments
505 0 $a 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 8 $a 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 8 $a 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
655 0 $a Electronic books. $2 local. $3 214472
856 4 0 $u https://www.sciencedirect.com/science/book/9780128174678