| Literature DB >> 27104299 |
Alicia M Phelps1, Vincent S Chan, José G Napolitano, Scott W Krabbe, Jennifer M Schomaker1, Shashank Shekhar.
Abstract
An iridium-catalyzed method was developed for the synthesis of imidazo-fused pyrrolopyrazines. The presence or absence of a nitrogenated ligand controlled the outcome of the reaction, leading to simple β-keto amine products in the absence of added ligand and the cyclized 7- and 8-substituted-imidazo[1,2-a]pyrrolo[2,3-e]pyrazine products in the presence of ligand. This catalyst control was conserved across a variety of ylide and amine coupling partners. The substrate was shown to act as a ligand for the iridium catalyst in the absence of other ligands via NMR spectroscopy. Kinetic studies indicated that formation of the Ir-carbene was reversible and the slow step of the reaction. These mechanistic investigations suggest that the β-keto amine products form via an intramolecular carbene N-H insertion, and the imidazopyrrolopyrazines form via an intermolecular carbene N-H insertion.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27104299 DOI: 10.1021/acs.joc.6b00497
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354