Chemical Transformations of the Fungal Meroterpenoid Dhilirolide A Reveal Skeletal Degradation and Rearrangement Reactions with Biosynthetic Implications
Author:
Affiliation:
1. Departments of Chemistry and Earth, Ocean and Atmospheric Sciences, University of British Columbia, 2036 Main Mall, Vancouver, BC, Canada V6T 1Z1
2. Department of Chemistry, University of Colombo, Colombo 03, Sri Lanka
Funder
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02037
Reference10 articles.
1. Dhilirolides A−D, Meroterpenoids Produced in Culture by the Fruit-Infecting Fungus Penicillium purpurogenum Collected in Sri Lanka
2. Dhilirolides E–N, Meroterpenoids Produced in Culture by the Fungus Penicillium purpurogenum Collected in Sri Lanka: Structure Elucidation, Stable Isotope Feeding Studies, and Insecticidal Activity
3. Terretonin, a toxic compound from Aspergillus terreus
4. Berkeleydione and Berkeleytrione, New Bioactive Metabolites from an Acid Mine Organism
5. Bi(OTf)3-catalyzed Regioselective Ring Opening of Epoxides with Phenols: Facile Synthesis of 1,3-Diaryloxy-2-propanols
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1. A Fungal Promiscuous UbiA Prenyltransferase Expands the Structural Diversity of Chrodrimanin-Type Meroterpenoids;Organic Letters;2022-03-09
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