| Literature DB >> 26097000 |
Sepideh Sharif1, Richard P Rucker1, Nalin Chandrasoma1, David Mitchell2, Michael J Rodriguez2, Robert D J Froese3, Michael G Organ4.
Abstract
A single set of reaction conditions for the palladium-catalyzed amination of a wide variety of (hetero)aryl halides using primary alkyl amines has been developed. By combining the exceptionally high reactivity of the Pd-PEPPSI-IPent(Cl) catalyst (PEPPSI=pyridine enhanced precatalyst preparation, stabilization, and initiation) with the soluble and nonaggressive sodium salt of BHT (BHT=2,6-di-tert-butyl-hydroxytoluene), both six- and five-membered (hetero)aryl halides undergo efficient and selective amination.Entities:
Keywords: PEPPSI; amination; cross-coupling; palladium; selectivity
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Year: 2015 PMID: 26097000 DOI: 10.1002/anie.201502822
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336