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Several privileged starting materials that allow access to a variety of different heterocyclic scaffolds through judicious choice of reaction conditions (and coupling partner) have emerged. This microreview focuses on the development and use of four of these starting material types in cascade reactions involving the palladium‐ or copper‐catalysed formation of aromatic carbon–nitrogen, carbon–oxygen...
A series of trihalogenated alkenylbenzenes undergo consecutive palladium catalyzed inter- and intramolecular amination reactions to deliver a series of 1-functionalized mono-chloroindoles. 4-, 5-, 6- and 7-Chloroindoles can all be prepared; carbamates, anilines and amines can be employed as the N-nucleophile.
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