Total Synthesis and Determination of the Absolute Configuration of Rakicidin C
Author:
Affiliation:
1. The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin, 300350, People’s Republic of China
2. College of Chemistry, Nankai University, Tianjin, 300071, People’s Republic of China
Funder
Ministry of Education of the People's Republic of China
National Natural Science Foundation of China
Hundred Young Academic Leaders Program of Nankai University
Natual Science the Frontiers Science Center for New Organic Matter
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02476
Reference36 articles.
1. Pharmaceutically active secondary metabolites of microorganisms
2. Exploration of nature's chemodiversity: the role of secondary metabolites as leads in drug development
3. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019
4. Rakicidins, New Cytotoxic Lipopeptides from Micromonospora sp. Fermentation, Isolation and Characterization.
5. Complete Stereochemistry and Preliminary Structure–Activity Relationship of Rakicidin A, a Hypoxia-Selective Cytotoxin from Micromonospora sp.
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