Literature DB >> 27424485

The Quest for Palladium-Catalysed Alkyl-Nitrogen Bond Formation.

Kilian Muñiz1,2, Claudio Martínez1, Álvaro Iglesias1.   

Abstract

Our interest in the development of transition-metal catalysis for the realisation of vicinal diamination reactions of alkenes started about a decade ago. A number of successful transformations in this area have been developed using palladium catalysis. As a challenging aspect of major importance, the palladium-catalysed coupling of alkyl-nitrogen bonds constitutes the second step in diaminations of alkenes. We here discuss the details that led us to consider high-oxidation-state palladium catalysis as a key feature in such C-N bond-forming reactions. This work discusses both our own contributions and the ones from colleagues and combines the discussion of catalytic reactions and stoichiometric control experiments. It demonstrates that reductive alkyl-nitrogen bond formation from palladium(IV) proceeds with a low activation barrier and through a linear transition state of nucleophilic displacement.
© 2016 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkenes; amination; oxidation; palladium; reductive elimination

Year:  2016        PMID: 27424485     DOI: 10.1002/tcr.201600073

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  2 in total

Review 1.  Hypervalent Iodine Reagents in High Valent Transition Metal Chemistry.

Authors:  Felipe Cesar Sousa E Silva; Anthony F Tierno; Sarah E Wengryniuk
Journal:  Molecules       Date:  2017-05-12       Impact factor: 4.411

2.  Photoinduced Olefin Diamination with Alkylamines.

Authors:  Sebastian Govaerts; Lucrezia Angelini; Charlotte Hampton; Laia Malet-Sanz; Alessandro Ruffoni; Daniele Leonori
Journal:  Angew Chem Int Ed Engl       Date:  2020-06-09       Impact factor: 16.823

  2 in total

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