| Literature DB >> 29205717 |
Qingquan Lu1, Sara Cembellín1, Steffen Greßies1, Santanu Singha1, Constantin G Daniliuc1, Frank Glorius1.
Abstract
An unprecedented MnI -catalyzed (2-indolyl)methylation of heteroarenes is reported. This method makes use of an aromatizing cascade strategy to install a (2-indolyl)methyl group into target molecules, thereby leading to the expedient synthesis of previously challenging and important unsymmetrical diheteroarylmethanes, in particular bis(2-indolyl)methanes. The proposed cascade process comprises the reorganization of multiple bonds with controlled regioselectivity and high atom economy and can be performed on a gram-scale. Furthermore, a metal-free C-H propargylation is observed. The diverse application of this method is also demonstrated.Entities:
Keywords: (2-indolyl)methylation; C−H activation; diheteroarylmethane derivatives; ethynyl benzoxazinanone; manganese
Year: 2018 PMID: 29205717 DOI: 10.1002/anie.201710060
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336