Recent developments in the synthesis of nitrogen-containing heterocycles from β-aminovinyl esters/ketones as C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C–N donors
C–N donors                                                    
    
                    Abstract
Nitrogen-containing heterocycles are ubiquitous fragments of numerous natural products, pharmaceuticals, designed bioactive drug candidates and agrochemicals. During the past few decades, these compounds have received considerable attention from the synthetic chemistry community, and great efforts have been focused on the development of concise and efficient methods for the synthesis of these heterocyclic skeletons. In this review, we summarize a diverse range of synthetic methods employing β-aminovinyl esters(ketones) as key C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) C–N-synthons to furnish useful bioactive heterocyclic frameworks, such as quinolines, pyridines, pyrazines, pyrroles, indoles, oxazoles, imidazoles, thiazoles, isothiazoles, pyrazoles, triazoles, and azepines, thus offering new opportunities and expanding the toolbox of synthetic chemistry reactions.
C–N-synthons to furnish useful bioactive heterocyclic frameworks, such as quinolines, pyridines, pyrazines, pyrroles, indoles, oxazoles, imidazoles, thiazoles, isothiazoles, pyrazoles, triazoles, and azepines, thus offering new opportunities and expanding the toolbox of synthetic chemistry reactions.
- This article is part of the themed collections: Synthetic methodology in OBC and Catalysis & biocatalysis in OBC
 
                




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        ![[double bond, length as m-dash]](https://www.rsc.org/images/entities/h2_char_e001.gif) C–N donors
C–N donors