Highly Reactive Glycosylation with 1-<i>O-</i>(Methylthio)thiocarbonyl Glycosyl Donors under Acidic to Neutral Reaction Conditions-Reference-Cited by-同舟云学术

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Highly Reactive Glycosylation with 1-O-(Methylthio)thiocarbonyl Glycosyl Donors under Acidic to Neutral Reaction Conditions

Published:2024-09-13 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Luo Tao¹,Zhang Guo-Hui¹,Guo Yang-Fan¹,Dong Hai¹^ORCID

Affiliation:

1. Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medica, School of Chemistry & Chemical Engineering, Huazhong University of Science & Technology, Luoyu Road 1037, Wuhan 430074, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01740

Reference55 articles.

1. Carbohydrates in Chemistry and Biology

2. Regioselective one-pot protection of carbohydrates

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

4. Regio/Stereoselective Glycosylation of Diol and Polyol Acceptors in Efficient Synthesis of Neu5Ac-α-2,3-LacNPhth Trisaccharide

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