Glycosylation with ulosonates under Mitsunobu conditions: scope and limitations-Reference-Cited by-同舟云学术

Glycosylation with ulosonates under Mitsunobu conditions: scope and limitations

Published:2020 Issue:34 Volume:44 Page:14463-14476
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kánya Nándor¹²³⁴^ORCID,Kun Sándor¹²³⁴^ORCID,Batta Gyula¹²³⁴^ORCID,Somsák László¹²³⁴^ORCID

Affiliation:

1. Department of Organic Chemistry

2. University of Debrecen

3. H-4002 Debrecen

4. Hungary

Abstract

Mitsunobu reactions on highly hindered tertiary type hydroxy groups of ulosonates: from 47 NuH compounds O-, N-, and S-nucleophiles gave the corresponding ulosidonates in 30–78% yields, while C-nucleophiles were unreactive.

Funder

European Regional Development Fund

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/D0NJ03044A

Reference36 articles.

1. Mitsunobu and Related Reactions: Advances and Applications

2. The Mitsunobu reaction in the 21st century

3. Anomeric modification of carbohydrates using the Mitsunobu reaction

4. A Mitsunobu route to C-glycosides

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