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Stereoselective Synthesis of cis - and trans -2,3-Disubstituted Tetrahydrofurans via Oxonium−Prins Cyclization: Access to the Cordigol Ring System

✍ Scribed by Spivey, Alan C.; Laraia, Luca; Bayly, Andrew R.; Rzepa, Henry S.; White, Andrew J. P.

Book ID
126962620
Publisher
American Chemical Society
Year
2010
Tongue
English
Weight
418 KB
Volume
12
Category
Article
ISSN
1523-7060

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ChemInform Abstract: Stereoselective Syn
ChemInform Abstract: Stereoselective Synthesis of cis- and trans-2,3-Disubstituted Tetrahydrofurans via Oxonium—Prins Cyclization: Access to the Cordigol Ring System.
✍ Alan C. Spivey; Luca Laraia; Andrew R. Bayly; Henry S. Rzepa; Andrew J. P. White 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 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

Diastereoselective construction of cis 2
Diastereoselective construction of cis 2,6-disubstituted tetrahydropyran rings via In(OTf)3-catalyzed intramolecular 2,5-oxonium-ene cyclization: synthetic studies towards the total synthesis of zampanolide and dactylolide
✍ Teck-Peng Loh; Jian-Ying Yang; Li-Chun Feng; Yan Zhou 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 129 KB

Diastereoselective construction of 2,6-disubstituted tetrahydropyrans with an exocyclic double bond was achieved via the In(OTf) 3 -catalyzed intramolecular 2,5-oxonium-ene cyclization. Its application was further demonstrated by the synthesis of a common intermediate for both zampanolide and dactyl