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Synthesis of (R)-(+)-Tanikolide, a Toxic and Antifungal δ-Lactone from the Marine Cyanobacterium Lyngbya majuscula

✍ Scribed by Matsuo, Keizo; Hikita, Junko; Nishiwaki, Keiji

Book ID
118276587
Publisher
Japan Institute of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
659 KB
Volume
83
Category
Article
ISSN
0385-5414

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📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of (R)-(+
ChemInform Abstract: Synthesis of (R)-(+)-Tanikolide, a Toxic and Antifungal δ-Lactone from the Marine Cyanobacterium Lyngbya majuscula.
✍ Keizo Matsuo; Junko Hikita; Keiji Nishiwaki 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

## Abstract Starting from the known lactol (I) and using its stereogenic center at C‐4, title compound (VI), a brine‐shrimp toxic and antifungal marine metabolite, is obtained in a 5‐step procedure.

ChemInform Abstract: The First Synthesis
ChemInform Abstract: The First Synthesis of (+)-Tanikolide, a Toxic and Antifungal Lactone from the Marine Cyanobacterium Lyngbya majuscula.
✍ Regina Mikie Kanada; Takahiko Taniguchi; Kunio Ogasawara 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

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Total synthesis of lyngbyabellin A, a po
Total synthesis of lyngbyabellin A, a potent cytotoxic metabolite from the marine cyanobacterium Lyngbya majuscula
✍ Fumiaki Yokokawa; Hirofumi Sameshima; Takayuki Shioiri 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 138 KB

The first total synthesis of lyngbyabellin A, a novel peptolide from the marine cyanobacterium Lyngbya majuscula, is described. Both functionalized thiazole carboxylic acid units were synthesized using our CMD (chemical manganese dioxide) oxidation from the corresponding thiazolidines. The asymmetri