On the generality of the superarmament of glycosyl donors-Reference-Cited by-同舟云学术

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On the generality of the superarmament of glycosyl donors

Published:2018 Issue:13 Volume:16 Page:2269-2276
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Poulsen Lulu Teressa¹²³⁴,Heuckendorff Mads¹²³⁴^ORCID,Jensen Henrik H.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Aarhus University

3. 8000 Aarhus C

4. Denmark

Abstract

We establish that the electronic superarmament of 2-OBz thioglucoside glycosyl donors under NIS/TfOH activation is not a general phenomenon.

Funder

Villum Fonden

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB02966G

Reference36 articles.

1. Ueber die Glucoside der Alkohole

2. New Principles for Glycoside-Bond Formation

3. Common side reactions of the glycosyl donor in chemical glycosylation

4. Realizing the promise of chemical glycobiology

5. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of Superarmed Thioglycosides via the Ring Opening of 1,2-Orthoesters;Synlett;2023-07-18

2. Anomeric Thioglycosides Give Different Anomeric Product Distributions under NIS/TfOH Activation;The Journal of Organic Chemistry;2022-03-03

3. How do Various Reaction Parameters Influence Anomeric Selectivity in Chemical Glycosylation with Thioglycosides and NIS/TfOH Activation?;European Journal of Organic Chemistry;2021-06-14

4. Conformational Lock of Glycosyl Donors Using Cyclic Carbamates;European Journal of Organic Chemistry;2020-10-02

5. Mechanisms of Stereodirecting Participation and Ester Migration from Near and Far in Glycosylation and Related Reactions;Chemical Reviews;2020-07-05

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