Anomerization of Methyl Glycosides by Acid-Catalysed Methanolysis: Trapping of Intermediates-Reference-Cited by-同舟云学术

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Anomerization of Methyl Glycosides by Acid-Catalysed Methanolysis: Trapping of Intermediates

Published:1999-01-01 Issue:1 Volume:18 Page:31-40
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Garegg Per J.¹²³⁴,Johansson Karl-Jonas¹²³⁴,Konradsson Peter¹²³⁴,Lindberg Bengt¹²³⁴

Affiliation:

1. a Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , S-10691 Stockholm, Sweden

2. b Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , S-10691 Stockholm, Sweden

3. c Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , S-10691 Stockholm, Sweden

4. d Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , S-10691 Stockholm, Sweden

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/07328309908543976

Reference27 articles.

1. Mechanism in carbohydrate chemistry

2. Reactions at high pressure. Part 8. The mechanisms of acid catalysed hydrolyses of glycosides

3. The acid hydrolysis of alkyl β-D-galactopyranosides

4. 18O and secondary2H kinetic isotope effects confirm the existence of two pathways for acid-catalysed hydrolyses of α-arabinofuranosides

5. The acid-catalyzed hydrolysis of β-d-xylofuranosides

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1. An experimental and theoretical study on stereocontrolled glycosylations by a “one-pot” procedure;Organic Chemistry Frontiers;2022

2. Synthesis and Fungicidal Activity ofD-Ribose andD-Xylose with Hydantion;Chinese Journal of Organic Chemistry;2014

3. Reaction kinetics and mechanism of acid-catalyzed anomerization of 1-O-acetyl-2,3,5-tri-O-benzoyl-l-ribofuranose;Carbohydrate Research;2009-06

4. Formation of the Glycosidic Linkage;Carbohydrates: The Essential Molecules of Life;2009

5. Facile Approach to 2-Acetamido-2-deoxy-β-d-Glucopyranosides via a Furanosyl Oxazoline;Organic Letters;2005-08-11

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