O-Glycosylation Enabled by N-(Glycosyloxy)acetamides-Reference-Cited by-同舟云学术

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O-Glycosylation Enabled by N-(Glycosyloxy)acetamides

Published:2018-06-25 Issue:15 Volume:83 Page:8292-8303
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Miao¹²,Li Bo-Han²,Xiong De-Cai²³^ORCID,Ye Xin-Shan¹²^ORCID

Affiliation:

1. National Research Center for Carbohydrate Synthesis, Jiangxi Normal University, Nanchang 330022, China

2. State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China

3. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China

Funder

National Natural Science Foundation of China

State Key Laboratory of Drug Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01003

Reference68 articles.

1. Chemical Glycobiology

2. Glycosylation and the Immune System

3. Synthesis and medical applications of oligosaccharides

4. Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research

5. Strategies for analysis of glycoprotein glycosylation

Cited by 11 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. The impact of N-glycans on the immune response of plant-produced SARS-CoV-2 RBD-Fc proteins;Biotechnology Reports;2024-09

2. Thioglycoside-based glycosylations in oligosaccharide synthesis;Synthetic Strategies in Carbohydrate Chemistry;2024

3. Efficient and versatile formation of glycosidic bonds via catalytic strain-release glycosylation with glycosyl ortho−2,2-dimethoxycarbonylcyclopropylbenzoate donors;Nature Communications;2023-07-07

4. Unusual promoters and leaving groups in glycosylation reactions: The evolution of carbohydrate synthesis;Carbohydrate Research;2022-09

5. Conversion of Glycals to 2,3‐Di‐Substituted‐3‐Deoxy‐Glycals by N‐(Glycosyloxy) Acetamides‐assisted C‐2‐Alkenylation and C‐3‐Nucleophilic Substitution;Chemistry – An Asian Journal;2022-05-23

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