Journal
ORGANIC LETTERS
Volume 21, Issue 12, Pages 4469-4474Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01296
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Funding
- FWO [Fund for Scientific Research-Flanders (Belgium)]
- Research Fund of the University of Leuven (KU Leuven)
- RUDN University Program 5-100
- China Scholarship Council (CSC)
- Hercules Foundation [AKUL/09/0035]
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A modular and streamlined synthetic strategy for the generation of bridged indole alkaloid-like heterocycles from easily available building blocks is elaborated. This approach utilizes an Ugi four-component reaction, establishing diversity, followed by an efficient cationic gold-triggered intramolecular cascade non-oxidative dearomative spirocarbocyclization/concerted [4 + 2] cyclization cascade, furnishing these architecturally complex and distinct bridged heterocyclic scaffolds with good diastereoselectivity.
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