| Literature DB >> 27594431 |
Alexander F G Maier1, Sebastian Tussing1, Tobias Schneider1, Ulrich Flörke2, Zheng-Wang Qu3, Stefan Grimme4, Jan Paradies5.
Abstract
An acceptorless dehydrogenation of heterocycles catalyzed by frustrated Lewis pairs (FLPs) was developed. Oxidation with concomitant liberation of molecular hydrogen proceeded in high to excellent yields for N-protected indolines as well as four other substrate classes. The mechanism of this unprecedented FLP-catalyzed reaction was investigated by mechanistic studies, characterization of reaction intermediates by NMR spectroscopy and X-ray crystal analysis, and by quantum-mechanical calculations. Hydrogen liberation from the ammonium hydridoborate intermediate is the rate-determining step of the oxidation. The addition of a weaker Lewis acid as a hydride shuttle increased the reaction rate by a factor of 2.28 through a second catalytic cycle.Entities:
Keywords: 1,2-dihydroquinolines; 1,4-dihydropyridines; acceptorless dehydrogenation; frustrated Lewis pairs; indolines
Year: 2016 PMID: 27594431 DOI: 10.1002/anie.201606426
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336