Mild and General Protocol for Selective Deacetylation of Acetyl/Benzoyl-Protected Carbohydrates-Reference-Cited by-同舟云学术

Mild and General Protocol for Selective Deacetylation of Acetyl/Benzoyl-Protected Carbohydrates

Published:2024-07-02 Issue:14 Volume:89 Page:10021-10026
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Abramov Alexander A.¹,Zinin Alexander I.²,Kolotyrkina Natalya G.²,Kononov Leonid O.²^ORCID,Shatskiy Andrey³,Kärkäs Markus D.³^ORCID,Stepanova Elena V.¹³^ORCID

Affiliation:

1. Tomsk Polytechnic University, Lenin Avenue 30, 634050 Tomsk, Russia

2. Laboratory of Glycochemistry, N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prosp. 47, 119991 Moscow, Russia

3. Department of Chemistry, KTH Royal Institute of Technology, SE-100 44 Stockholm, Sweden

Funder

Centrum f?r idrottsforskning

Magnus Bergvalls Stiftelse

Kungliga Tekniska H?gskolan

Olle Engkvists Stiftelse

Ministry of Education and Science of the Russian Federation

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00900

Reference57 articles.

1. A General Strategy for Stereoselective Glycosylations

2. Exploring the Mechanism of Neighboring Group Assisted Glycosylation Reactions

3. Five Triisopropylsilyl Substituents in Ara‐β‐(1→2)‐Ara Disaccharide Glycosyl Donor Make Unselective Glycosylation Reaction Stereoselective

4. A Novel Glycosyl Donor with a Triisopropylsilyl Nonparticipating Group in Benzyl-Free Stereoselective 1,2-cis-Galactosylation

5. β-Directing Effect of Electron-Withdrawing Groups at O-3, O-4, and O-6 Positions and α-Directing Effect by Remote Participation of 3-O-Acyl and 6-O-Acetyl Groups of Donors in Mannopyranosylations