| Literature DB >> 29668069 |
Christoph Bäumler1, Rhett Kempe1.
Abstract
The "replacement" of noble metals by earth abundant metals is a desirable aim in catalysis and a possible way of conserving rare elements. The "replacement" is especially attractive if novel selectivity patterns are observed permitting the development of novel coupling reactions. Herein, we report on a novel, robust and reusable iron catalyst, which permits the selective hydrogenation of nitroarenes in the presence of hydrogenation-sensitive functional groups. Based on the selectivity pattern observed, the direct iron-catalyzed synthesis of imines and benzimidazoles from nitroarenes and aldehydes becomes feasible. In addition, we introduce the direct synthesis of quinoxalines from nitroarenes and diketones applying our catalyst.Entities:
Keywords: benzimidazoles; hydrogenation; imines; iron; quinoxalines
Year: 2018 PMID: 29668069 DOI: 10.1002/chem.201801525
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236