| Literature DB >> 30070744 |
Sangil Han1, Prashant Chakrasali2,3, Jihye Park1, Hyunjung Oh1, Saegun Kim1, Kyuneun Kim2,3, Ashok Kumar Pandey1, Sang Hoon Han1, Soo Bong Han2,3, In Su Kim1.
Abstract
The ability to alkylate pyridines and quinolines is important for their further development as pharmaceuticals and agrochemicals, and for other purposes. Herein we describe the unprecedented reductive alkylation of pyridine and quinoline N-oxides using Wittig reagents. A wide range of pyridine and quinoline N-oxides were converted into C2-alkylated pyridines and quinolines with excellent site selectivity and functional-group compatibility. Sequential C-H functionalization reactions of pyridine and quinoline N-oxides highlight the utility of the developed method. Detailed labeling experiments were performed to elucidate the mechanism of this process.Entities:
Keywords: Wittig reagents; alkylation; methylation; pyridine N-oxides; regioselectivity
Year: 2018 PMID: 30070744 DOI: 10.1002/anie.201807159
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336