A Unified Synthetic Strategy for the Indolopyridine Alkaloid Group
✍ Scribed by Rodolfo Lavilla; Francisco Gullón; Joan Bosch
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 164 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-193X
No coin nor oath required. For personal study only.
✦ Synopsis
Thermal or acetyl chloride induced cyclization of bromo-intermediate, palladium-catalyzed reactions allow the total synthesis of indolopyridine alkaloids 1-6. enamide 10 affords the pentacyclic derivative 12 with high yield and regioselectivity. From this common synthetic Extensive studies on the total synthesis of these alkaloids [a] Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona,
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## Abstract A unified synthetic strategy for the asymmetric syntheses of the natural products diversonol and lachnone C was developed by using the domino vinylogous aldol–oxa‐Michael reaction as the enantioselective key step. Further transformations include dihydroxylation, lactol‐opening by a Witt