Literature DB >> 26097000

Selective Monoarylation of Primary Amines Using the Pd-PEPPSI-IPent(Cl) Precatalyst.

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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  PEPPSI; amination; cross-coupling; palladium; selectivity

Mesh:

Substances:

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


  4 in total

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