Synthesis of C4‐Acyl‐tetrofuranosides and C5‐Acyl‐pentopyranosides Enabled by the Liebeskind‐Srogl Cross‐Coupling Reaction-Reference-Cited by-同舟云学术

Synthesis of C4‐Acyl‐tetrofuranosides and C5‐Acyl‐pentopyranosides Enabled by the Liebeskind‐Srogl Cross‐Coupling Reaction

Published:2022-03-04 Issue:4 Volume:11 Page:
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J of Organic Chemis

Author:

Xu Linhua¹,Hou Zijiao¹,Ma Xian¹,Ma Yixuan¹,Wang Jianjun¹,Zhang Xinxin¹,Wang Peng¹,Li Ming¹²³^ORCID

Affiliation:

1. Key Laboratory of Marine Medicine, Chinese Ministry of Education School of Medicine and Pharmacy Ocean University of China Qingdao 266003 P. R. China

2. Laboratory for Marine Drugs and Bioproducts Pilot National for Marine Science and Technology Qingdao 266237 P. R. China

3. Shandong Provincial Key Laboratory of Glycoscience and Glycotechnology School of Medicine and Pharmacy Ocean University of China Qingdao 266003 P. R. China

Funder

National Natural Science Foundation of China

National Natural Science Foundation of China-Shandong Joint Fund

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202100665

Reference83 articles.

2. Glycobiology: Toward Understanding the Function of Sugars

3. Automated synthesis of oligosaccharides as a basis for drug discovery

4. Application of Mono- and Disaccharides in Drug Targeting and Efficacy

5. Toward a Carbohydrate-Based Chemistry: Progress in the Development of General-Purpose Chiral Synthons from Carbohydrates

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