Asymmetric Total Synthesis of Botcinins C, D, and F
Author:
Affiliation:
1. Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol801066y
Reference12 articles.
1. Botcinins E and F and Botcinolide from Botrytis cinerea and Structural Revision of Botcinolides
2. Botcinins A, B, C, and D, Metabolites Produced by Botrytis cinerea, and Their Antifungal Activity against Magnaporthe grisea, a Pathogen of Rice Blast Disease
3. Stereoselective Total Synthesis of the Proposed Structure of 2-Epibotcinolide
4. Studies directed towards the total synthesis of botcinic acid, the revised structure of botcinolide: synthesis of the highly substituted tetrahydropyran moiety
5. Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systems
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