The Naturally Occurring Ketene Acetal Benesudon: Total Synthesis and Assignment of Relative and Absolute Stereochemistry
Author:
Affiliation:
1. Chemistry Department, University of Alberta, Edmonton, Alberta T6G 2G2, Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo801028y
Reference47 articles.
1. Benesudon, a New Antibiotic Fungal Metabolite from Cultures of Mollisia benesuada (Tul.) Phill.
2. Ketene Acetal and Spiroacetal Constituents of the Marine Fungus Aigialus parvus BCC 5311
3. Oxidative Decarboxylation as a Route to Ketene Acetals: Assignment of Relative and Absolute Stereochemistry to the Fungal Metabolite Benesudon by Total Synthesis
4. Ketene Acetals. XXXV. Cyclic Ketene Acetals and Orthoesters from 2,2-Dimethoxy-2,3-dihydropyran
5. Synthesis of Polycyclic Structures by the Diels−Alder Reaction of Inner-Outer-Ring 1,3-Bis(trimethylsilyloxy)dienes
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