Reaction Rate and Stereoselectivity Enhancement in Glycosidations with O-Glycosyl Trihaloacetimidate Donors due to Catalysis by a Lewis Acid–Nitrile Cooperative Effect-Reference-Cited by-同舟云学术

Reaction Rate and Stereoselectivity Enhancement in Glycosidations with O-Glycosyl Trihaloacetimidate Donors due to Catalysis by a Lewis Acid–Nitrile Cooperative Effect

Published:2024-05-28 Issue:11 Volume:89 Page:7865-7876
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Tianlu¹^ORCID,Li Tong¹,Yang Yue¹,Qiu Yongshun¹,Liu Yingguo²^ORCID,Zhang Miaomiao¹,Zhuang Haoru¹,Schmidt Richard R.³^ORCID,Peng Peng¹^ORCID

Affiliation:

1. National Glycoengineering Research Center, Shandong Technology Innovation Center of Carbohydrate, NMPA Key Laboratory for Quality Research and Evaluation of Carbohydrate Based Medicine, Key Laboratory of Chemical Biology (Ministry of Education), Shandong University, Shandong 266237, China

2. Division of Molecular Catalysis and Synthesis, Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450000, China

3. Department of Chemistry, University of Konstanz, Konstanz D-78457, Germany

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Youth Innovation Technology Project of Higher School in Shandong Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00554

Reference67 articles.

1. New Principles for Glycoside-Bond Formation

2. “One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates

3. Oligosaccharide Synthesis and Translational Innovation

4. Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research

5. Acceptor reactivity in glycosylation reactions

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