N-Glycosylation with sulfoxide donors for the synthesis of peptidonucleosides-Reference-Cited by-同舟云学术

N-Glycosylation with sulfoxide donors for the synthesis of peptidonucleosides

Published:2021 Issue:19 Volume:19 Page:4285-4291
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Beretta Margaux¹²³⁴⁵,Rouchaud Emilie¹²³⁴⁵,Nicolas Lionel⁶⁷⁸⁹¹⁰,Vors Jean-Pierre⁶⁷⁸⁹¹⁰,Dröge Thomas⁶⁷¹¹¹²,Es-Sayed Mazen⁶⁷¹¹¹²,Beau Jean-Marie¹²³⁴⁵^ORCID,Norsikian Stéphanie¹²³⁴⁵^ORCID

Affiliation:

1. Université Paris-Saclay

2. CNRS

3. Institut de Chimie des Substances Naturelles

4. UPR 2301

5. Gif-sur-Yvette

6. Bayer CropScience

7. Disease Control Chemistry

8. Centre de Recherche de La Dargoire

9. 69009 Lyon

10. France

11. 40789 Monheim am Rhein

12. Germany

Abstract

The activation of sulfoxide donors in the glycosylation of pyrimidine bases led efficiently to glycosylated adducts that were converted into peptidonucleosides, the analogues of gougerotin.

Funder

Centre National de la Recherche Scientifique

Bayer CropScience

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00493J

Reference31 articles.

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4. Nucleosides. LXXV. Synthetic studies on nucleoside antibiotics. 9. Total synthesis of gougerotin

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