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Reductive C2‐Alkylation of Pyridine and Quinoline N‐Oxides Using Wittig Reagents.
- Source :
-
Angewandte Chemie International Edition . 9/24/2018, Vol. 57 Issue 39, p12737-12740. 4p. - Publication Year :
- 2018
-
Abstract
- 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. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CHEMICAL reactions
*ALKYLATION
*PYRIDINE
*QUINOLINE
*WITTIG reaction
Subjects
Details
- Language :
- English
- ISSN :
- 14337851
- Volume :
- 57
- Issue :
- 39
- Database :
- Academic Search Index
- Journal :
- Angewandte Chemie International Edition
- Publication Type :
- Academic Journal
- Accession number :
- 131861624
- Full Text :
- https://doi.org/10.1002/anie.201807159