| Literature DB >> 28586128 |
Jesús Sanjosé-Orduna1, Daniel Gallego1, Alèria Garcia-Roca1, Eddy Martin1, Jordi Benet-Buchholz1, Mónica H Pérez-Temprano1.
Abstract
Despite Cp*CoIII catalysts having emerged as a very attractive alternative to noble transition metals for the construction of heterocyclic scaffolds through C-H activation, the structure of the reactive species remains uncertain. Herein, we report the identification and unambiguous characterization of two long-sought cyclometalated Cp*CoIII complexes that have been proposed as key intermediates in C-H functionalization reactions. The addition of MeCN as a stabilizing ligand plays a crucial role, allowing the access to otherwise highly reactive species. Mechanistic investigations demonstrate the intermediacy of these species in oxidative annulations with alkynes, including the direct observation, under catalytic conditions, of a previously elusive post-migratory insertion seven-membered cobaltacycle.Entities:
Keywords: C−H activation; cobalt catalysis; heterocycles; reaction mechanisms; structure elucidation
Year: 2017 PMID: 28586128 DOI: 10.1002/anie.201704744
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336