Meroterpenoid Synthesis via Sequential Polyketide Aromatization and Radical Anion Cascade Triene Cyclization: Biomimetic Total Syntheses of Austalide Natural Products
Author:
Affiliation:
1. Department of Chemistry, Imperial College, Molecular Sciences Research Hub, White City Campus, Wood Lane, London W12 0BZ, England
Funder
Engineering and Physical Sciences Research Council
GlaxoSmithKline
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00142
Reference23 articles.
1. Structures of the austalides A–E, five noval toxic metabolites from Aspergillus ustus
2. Metabolites of Aspergillus ustus. Part 1. Application of the heteronuclear selective population inversion (SPI) n.m.r. technique to the structure elucidation of the austalides A–F, novel ortho ester meroterpenoids
3. Metabolites of Aspergillus ustus. Part 2. Stereoelectronic control in the acid-catalysed hydrolysis of the ortho ester moiety in austalides A–F
4. Metabolites of Aspergillus ustus. Part 3. Structure elucidation of austalides G–L
5. New Austalides from the Sponge-Associated Fungus Aspergillus sp.
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