α-Selective glycosylations using glycosyl N-(ortho-methoxyphenyl)trifluoroacetimidates-Reference-Cited by-同舟云学术

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α-Selective glycosylations using glycosyl N-(ortho-methoxyphenyl)trifluoroacetimidates

Published:2020 Issue:10 Volume:18 Page:1918-1925
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kowalska Karolina¹²³⁴⁵,Pedersen Christian Marcus¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Copenhagen

3. DK-2100 Copenhagen

4. Denmark

5. Faculty of Chemistry

Abstract

β-Selective acetimidate formation followed by α-selective catalytic activation.

Funder

European Social Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/C9OB02696G

Reference34 articles.

1. Catalytic Glycosylations in Oligosaccharide Synthesis

2. Facile Synthesis ofα- andβ-O-Glycosyl Imidates; Preparation of Glycosides and Disaccharides

3. AN EFFICIENT METHOD FOR GLUCOSYLATION OF HYDROXY COMPOUNDS USING GLUCOPYRANOSYL FLUORIDE

4. Propargyl Glycosides as Stable Glycosyl Donors: Anomeric Activation and Glycoside Syntheses

5. An efficient glycosylation protocol with glycosyl ortho-alkynylbenzoates as donors under the catalysis of Ph3PAuOTf

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