An Efficient Synthesis of the Protected Carbohydrate Moiety of Brasilicardin A
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, 405 Hilgard Avenue, Los Angeles, California 90095, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol2013704
Reference19 articles.
1. Brasilicardin A. A Novel Tricyclic Metabolite with Potent Immunosuppressive Activity from Actinomycete Nocardia brasiliensis
2. Brasilicardins B–D, new tricyclic terpernoids from actinomycete Nocardia brasiliensis
3. SAR studies of brasilicardin A for immunosuppressive and cytotoxic activities
4. Brasilicardin A, a New Terpenoid Antibiotic from Pathogenic Nocardia brasiliensis: Fermentation, Isolation and Biological Activity.
5. Facile Synthesis ofα- andβ-O-Glycosyl Imidates; Preparation of Glycosides and Disaccharides
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1. A Journey to the Total Synthesis of Brasilicardins;Modern Natural Product Synthesis;2024
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3. Synthesis of a Complex Brasilicardin Analogue Utilizing a Cobalt-Catalyzed MHAT-Induced Radical Bicyclization Reaction;Organic Letters;2023-05-04
4. Selective mono-de-O-acetylation of the per-O-acetylated brasilicardin carbohydrate side chain;Carbohydrate Research;2021-06
5. Genetic Engineering in Combination with Semi‐Synthesis Leads to a New Route for Gram‐Scale Production of the Immunosuppressive Natural Product Brasilicardin A;Angewandte Chemie International Edition;2021-05
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