Palladium-catalysed coupling of aryl and vinyl triflates or halides with 2-ethynylaniline: An efficient route to functionalized 2-substituted indoles
β Scribed by A. Arcadi; S. Cacchi; F. Marinelli
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 247 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The palladium(O)-catalysed coupling of aryl and vinyl triflates or halides with the easily available 2-ethynylaniline, followed by a palladium(IIl-catalysed cyclization step, provides an efficient and very versatile procedure for the synthesis of functionalyzed E-substituted indoles.
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## The palladium-caralysed cyclizarion of o-alkynyltriftwroaceranilides with vinyl rrrJares and atyl halides produces 2,3-disubsrituted indoles in.good 10 high yield.
Palladium-Catalysed Vinylic Substitution of Aryl
Highly efficient palladium-catalyzed couplings of alkenyl tosylates with organoindium reagents under mild conditions are described, which give rise to 4-substituted coumarins, 2(5H)-furanones, and pyrones in good to excellent yields.