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ChemInform Abstract: Synthetic Microbial Chemistry. Part 37. Synthesis and Absolute Configuration of Nocardione A and B, Furano-o-naphthoquinone-Type Metabolites of Nocardia sp. with Antifungal, Cytotoxic, and Enzyme Inhibitory Activities.

✍ Scribed by Yoshihisa Tanada; Kenji Mori

Publisher: John Wiley and Sons
Year: 2010
Weight: 27 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200218216

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Synthesis and Absolute Configuration of

Synthesis and Absolute Configuration of Nocardione A and B, Furano-o-naphthoquinone-Type Metabolites of Nocardia sp. with Antifungal, Cytotoxic, and Enzyme Inhibitory Activities

✍ Yoshihisa Tanada; Kenji Mori 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 323 KB

1), (S)-(-)-nocardione A, and (R)-(+)-nocardione B (2) were synthesized by starting from the enantiomers of propylene oxide and 5-benzyloxy (or methoxy)-