ArticleTetrahedron letters2015
A Practical, Multi-gram Synthesis of (±)-Herbindole A, (±)-Herbindole B, and (±)-Herbindole C from a Common Intermediate via 6,7-Indole Aryne Cycloaddition and Pd(0)-Catalyzed Cross-Coupling Reactions.
Article in Tetrahedron letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Total Synthesis of (+)-Raputindole A: An Iridium-Catalyzed Cyclization Approach.Organic letters · 2020Article
- Synthesis of the tricyclic indole alkaloids, dilemmaones A and B.Tetrahedron · 2019Article
- Six Trikentrin-like Cyclopentanoindoles from Trikentrion flabelliforme. Absolute Structural Assignment by NMR and ECD.The Journal of organic chemistry · 2018Article
- Expanding the Strained Alkyne Toolbox: Generation and Utility of Oxygen-Containing Strained Alkynes.Journal of the American Chemical Society · 2016Article
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Authors and funding
3 authors.
Funding
Abstract
A practical, multi-gram 10-step synthesis of racemic herbindole A, B, and C from a common intermediate is described. The key step features a remarkably regioselective C-7 metal-halogen exchange and elimination from a Bartoli-generated
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