Preparation of the cde-ring system of pleurotin and geogenine via a stereoselective free radical cyclization
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (32) , 3749-3752
- https://doi.org/10.1016/s0040-4039(00)89241-2
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- New syntheses of carbocycles from carbohydrates. Cyclization of radicals derived from unsaturated halo sugarsThe Journal of Organic Chemistry, 1985
- Control of ring junction stereochemistry via radical cyclizationJournal of the American Chemical Society, 1985
- On the stereochemical course of cuprate-mediated homoconjugate addition to an activated cyclopropaneTetrahedron Letters, 1984
- A new entry to highly functionalized perhydroindans via free radical cyclizationsThe Journal of Organic Chemistry, 1983
- Structure de la géogénine, nouvelle quinone lactone isolée de Hohenbuehelia goegeniusActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1981
- Dissolving metal reduction of esters to alkanes. A method for the deoxygenation of alcoholsJournal of the Chemical Society, Perkin Transactions 1, 1981
- Bioactivation as a Model for Drug Design Bioreductive AlkylationScience, 1977
- Structure de la pleurotine: Une benzoquinone extraite de pleurotus griseus.Tetrahedron Letters, 1974
- Protection of hydroxyl groups as tert-butyldimethylsilyl derivativesJournal of the American Chemical Society, 1972
- Enzymic formation of a tricyclic sesterterpene alcohol from mevalonic acid and all-trans-geranylfarnesyl pyrophosphateJournal of the Chemical Society D: Chemical Communications, 1969