| Literature DB >> 27424485 |
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.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