Approaches to the synthesis of cytochalasans. Part 5. Studies on the selectivity of the Diels‐Alder reaction leading to the tetrahydroiso‐indolinone sub‐unit
- 21 September 1983
- journal article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 66 (6), 1796-1805
- https://doi.org/10.1002/hlca.19830660619
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Crystal Structures of rac‐Methyl‐ (3R*, 3aS*, 4R*, 7R*, 7aR*)‐7‐Acetoxymethyl)‐3‐benzyl‐4,5‐dimethyl‐1‐oxo‐3a,4,7,7a‐tetrahydroisoindoline‐7a‐carboxylateHelvetica Chimica Acta, 1981
- Approaches to the Synthesis of Cytochalasans. Part 3. Synthesis of a substituted tetrahydroisoindolinone moiety possessing the same relative configuration as proxiphominHelvetica Chimica Acta, 1981
- Tetracyclines. 10. Chemical-structural properties of tetracycline derivatives. 5. A total synthesis and structural aspects of racemic 8-oxygenated tetracyclinesJournal of the American Chemical Society, 1979
- An approach to cytochalasins: Diels-Alder addition of .alpha.,.beta.-unsaturated imidesThe Journal of Organic Chemistry, 1978