Literature DB >> 30070744

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

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.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  2 in total

1.  Alkylation of Nitropyridines via Vicarious Nucleophilic Substitution.

Authors:  Damian Antoniak; Michał Barbasiewicz
Journal:  Org Lett       Date:  2022-01-03       Impact factor: 6.005

2.  Site-selective and metal-free C-H nitration of biologically relevant N-heterocycles.

Authors:  Junghyea Moon; Hyun Ku Ji; Nayoung Ko; Harin Oh; Min Seo Park; Suho Kim; Prithwish Ghosh; Neeraj Kumar Mishra; In Su Kim
Journal:  Arch Pharm Res       Date:  2021-10-18       Impact factor: 4.946

  2 in total

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