Resum
Copyright © 2018 American Chemical Society. A well-defined low-coordinate β-diketiminatocobalt(II) alkyl complex is reported as an active precatalyst for the selective alkene cyclohydroamination of unprotected primary amines under mild conditions (rt-90 °C). The reaction mechanism has been investigated by deuterium-labeling, kinetics, and stoichiometric experiments and in-depth computational DFT studies. On the basis of these studies, we propose a stepwise noninsertive mechanism that features a rate-determining nucleophilic attack of the amido group of a monomeric cobalt(II) amidoalkene-aminoalkene adduct intermediate to the noncoordinated pendant alkene followed by a rapid proton transfer from the coordinated aminoalkene to the cyclized adduct.
Idioma original | Anglès |
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Pàgines (de-a) | 4446-4451 |
Revista | ACS Catalysis |
Volum | 8 |
Número | 5 |
DOIs | |
Estat de la publicació | Publicada - 4 de maig 2018 |