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Total Synthesis of Palmarumycin CP 1 and (±)-Deoxypreussomerin A

✍ Scribed by Wipf, Peter; Jung, Jae-Kyu

Book ID: 121228388
Publisher: American Chemical Society
Year: 1998
Tongue: English
Weight: 44 KB
Volume: 63
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo980576v

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📜 SIMILAR VOLUMES

ChemInform Abstract: Total Synthesis of

ChemInform Abstract: Total Synthesis of Palmarumycin CP1 and (.+-.)-Deoxypreussomerin A.

✍ P. WIPF; J.-K. JUNG 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Synthesis and biological evaluation of d

Synthesis and biological evaluation of deoxypreussomerin A and palmarumycin CP1 and related naphthoquinone spiroketals

✍ Peter Wipf; Jae-Kyu Jung; Sonia Rodrı́guez; John S Lazo 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 280 KB

ChemInform Abstract: The Synthesis of 1,

ChemInform Abstract: The Synthesis of 1,8-Dihydroxynaphthalene-Derived Natural Products: Palmarumycin CP1, Palmarumycin CP2, Palmarumycin C11, CJ-12,371, Deoxypreussomerin A and Novel Analogues.

✍ Jacques P. Ragot; Christoph Steeneck; Marie-Lyne Alcaraz; Richard J. K. Taylor 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Synthesis and Biolo

ChemInform Abstract: Synthesis and Biological Evaluation of Deoxypreussomerin A and Palmarumycin CP1 and Related Naphthoquinone Spiroketals.

✍ Peter Wipf; Jae-Kyu Jung; Sonia Rodriguez; John S. Lazo 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

ChemInform Abstract: Total Syntheses of

ChemInform Abstract: Total Syntheses of Palmarumycins CP1 and CP2 and CJ-12,371: Novel Spiro-Ketal Fungal Metabolites.

✍ A. G. M. BARRETT; D. HAMPRECHT; T. MEYER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB

Syntheses of palmarumycin CP1 and CP2, C

Syntheses of palmarumycin CP1 and CP2, CJ-12,371 and novel analogues

✍ Jacques P Ragot; Marie-Lyne Alcaraz; Richard J.K Taylor 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 213 KB

Total syntheses of the title fungal metabolites are described via a route which utilises initial acetalisation with 1,8-dihydroxynaphthalene followed by elaboration of the ring A functionality. Novel analogues are also reported.