Synthesis of the Isoxazolo[4,3,2-de]phenanthridinone Moiety of the Parnafungins
Author:
Affiliation:
1. Department of Chemistry, MS 015, Brandeis University, Waltham, Massachusetts 02454-9110
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol901054r
Reference23 articles.
1. Isolation and Structure Elucidation of Parnafungins, Antifungal Natural Products that Inhibit mRNA Polyadenylation
2. PAP Inhibitor with In Vivo Efficacy Identified by Candida albicans Genetic Profiling of Natural Products
3. Application of Affinity Selection/Mass Spectrometry to Determine the Structural Isomer of Parnafungins Responsible for Binding Polyadenosine Polymerase
4. Isolation and structure elucidation of parnafungins C and D, isoxazolidinone-containing antifungal natural products
5. New Mono- and Dimeric Members of the Secalonic Acid Family: Blennolides A–G Isolated from the FungusBlennoria sp.
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