✦ LIBER ✦

Total synthesis of hibiscone C (gmelofuran)

✍ Scribed by Koft, Emil R.; Smith, Amos B.

Book ID: 127095670
Publisher: American Chemical Society
Year: 1982
Tongue: English
Weight: 407 KB
Volume: 104
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja00384a085

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intramolecular [2 + 2] photocyclizations

Intramolecular [2 + 2] photocyclizations. 2. Total synthesis of (.+-.)-hibiscone C (gmelofuran)

✍ Koft, Emil R.; Smith, Amos B. 📂 Article 📅 1984 🏛 American Chemical Society 🌐 English ⚖ 892 KB

Total synthesis of (±)-hibiscone C

✍ Sinziana Ungureanu; Maggie Meadows; Joel Smith; David B. Duff; James M. Burgess; 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 341 KB

Naturally occurring quinones. Part 27. S

Naturally occurring quinones. Part 27. Sesquiterpenoid quinones and related compounds from Hibiscus elatus: crystal structure of hibiscone C (gmelofuran)

✍ Ferreira, Margarida A.; King, Trevor J.; Ali, Sadaquat; Thomson, Ronald H. 📂 Article 📅 1980 🏛 Royal Society of Chemistry ⚖ 994 KB

ChemInform Abstract: An Efficient Synthe

ChemInform Abstract: An Efficient Synthesis of Racemic Hibiscone C.

✍ George A. Kraus; Zhiwen Wan 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

Total synthesis of (−)-betaenone C

✍ Akitami Ichihara; Shokyo Miki; Hirokazu Kawagishi; Sadao Sakamura 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 244 KB

Stereoselective synthesis of (-)-betaenone C through intramolecular Diels-Alder reaction has trade pssible to provide pertinent intermediates for the biosynthetic study of betaenones.

Total synthesis of (+)-crocacin C

✍ Tushar K Chakraborty; Sarva Jayaprakash 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 85 KB

The first synthesis of ( +)-crocacin C (3) in optically pure form is achieved following a convergent strategy. The synthesis also establishes the absolute stereochemistries of this novel class of potent antifungal and highly cytotoxic compounds. The naturally occurring crocacin C has (6S,7S,8R,9S) c