Determination of the absolute configurations of the stereogenic centers of ustilaginoidins by studying the biosynthetic monomers from a gene knockout mutant of Villosiclava virens
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-37941-5.pdf
Reference28 articles.
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2. Shibata, S. & Ogihara, Y. Metabolic products of fungi. XXIII. Ustilaginoidins. 3. The structure of ustilaginoidins B and C. Chem. Pharm. Bull. 11, 1576–1578 (1963).
3. Koyama, K. & Natori, S. Further characterization of seven bis(naphtho-γ-pyrone) congeners of ustilaginoidins, pigments of Claviceps virens (Ustilaginoidea virens). Chem. Pharm. Bull. 36, 146–152 (1988).
4. Lu, S. et al. Bioactive bis-naphtho-γ-pyrones from rice false smut pathogen Ustilaginoidea virens. J. Agric. Food Chem. 63, 3501–3508 (2015).
5. Sun, W. et al. New ustilaginoidins from rice false smut balls caused by Villosiclava virens and their phytotoxic and cytotoxic activities. J. Agric. Food Chem. 65, 5151–5160 (2017).
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