Selective Reduction Leading to 3,5-<i>cis</i>-3-Aminosugars: Synthesis and Stereoselective Glycosylation-Reference-Cited by-同舟云学术

Selective Reduction Leading to 3,5-cis-3-Aminosugars: Synthesis and Stereoselective Glycosylation

Published:2022-12-14 Issue:1 Volume:88 Page:727-731
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fu Dengxian¹,Zhang Shuxin¹,Xu Bingbing¹,Peng Peng²^ORCID,Wan Qian¹^ORCID,Zeng Jing¹²^ORCID

Affiliation:

1. Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan, Hubei 430030, P. R. China

2. Shandong Key Laboratory of Carbohydrate Chemistry and Glycobiology, Shandong University, Qingdao, Shandong 266237, P. R. China

Funder

Ministry of Education of the People's Republic of China

National Natural Science Foundation of China

Shandong Key Laboratory of Carbohydrate Chemistry and Glycobiology, Shandong University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02364

Reference61 articles.

1. Inhibition of ribosomal and RNA polymerase functions by rubradirin and its aglycone.

2. Syntheses of 2,3,6-trideoxy-3-amino- and 2,3,6-trideoxy-3-nitrohexoses

3. Synthesis and antitumor properties of new glycosides of daunomycinone and adriamycinone

4. A comprehensive review of glycosylated bacterial natural products

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