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Stereoselective Synthesis of Dihydropyrone-Containing Marine Natural Products. Total Synthesis and Structural Elucidation of (−)-Membrenone-C

✍ Scribed by Perkins, Michael V.; Sampson, Rebecca A.

Book ID
111918045
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
130 KB
Volume
3
Category
Article
ISSN
1523-7060

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📜 SIMILAR VOLUMES

ChemInform Abstract: Stereoselective Syn
ChemInform Abstract: Stereoselective Synthesis of Dihydropyrone-Containing Marine Natural Products. Total Synthesis and Structural Elucidation of (-)-Membrenone-C.
✍ Michael V. Perkins; Rebecca A. Sampson 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Stereoselective total synthesis of (±)-i
Stereoselective total synthesis of (±)-isolobophytolide, a marine cembranolide natural product
✍ James A. Marshall; Robert C. Andrews 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 277 KB

The total synthesis of ( Z!I l-isolobophytolide (20) has been achieved via a route involving piallvl oalladium initiated macrocvclization of sulfone ester 8 and subseauent carboxv inversion of the ma"cr&yclic acid 11 to introduce-the C-14 lactone oxygen. Lactone a-rnethylenatiok was effected by dehy