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Reductive C2‐Alkylation of Pyridine and Quinoline N‐Oxides Using Wittig Reagents.

Authors :
Han, Sangil
Chakrasali, Prashant
Park, Jihye
Oh, Hyunjung
Kim, Saegun
Kim, Kyuneun
Pandey, Ashok Kumar
Han, Sang Hoon
Han, Soo Bong
Kim, In Su
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]

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