Glycosylation in room temperature ionic liquid using unprotected and unactivated donors-Reference-Cited by-同舟云学术

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Glycosylation in room temperature ionic liquid using unprotected and unactivated donors

Published:2007-02 Issue:3-4 Volume:342 Page:614-620
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Park Tae-Joon,Weïwer Michel,Yuan Xuejun,Baytas Sultan N.,Munoz Eva M.,Murugesan Saravanababu,Linhardt Robert J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference15 articles.

1. Protecting Groups: Effects on Reactivity, Glycosylation Stereoselectivity, and Coupling Efficiency

2. Glycosyl Halides in Oligosaccharide Synthesis

3. Carbohydrates in Chemistry and Biology;Ernst,2000

4. Ueber die Glucoside der Alkohole

5. Nonionic Surfactants—Alkyl Polyglucosides;Balzer,2000

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1. Recent applications of ionic liquid-based tags in glycoscience;Carbohydrate Research;2022-10

2. Solid-Phase Synthesis of Polysaccharides from Unprotected Glucose Catalyzed by Hβ Zeolites;ACS Sustainable Chemistry & Engineering;2022-07-20

3. Growing Impact of Ionic Liquids in Carbohydrate Chemistry;Green Chemistry;2022

4. O-Glycoside Formation;Synthesis and Characterization of Glycosides;2022

5. Solvent‐Free Glycosylation from per‐ O ‐Acylated Donors Catalyzed by Methanesulfonic Acid;European Journal of Organic Chemistry;2021-11-04

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