The Synthesis of Pyrroles from Nitroolefins
The synthesis of pyrroles occupies a key place in synthetic organic chemistry due to the numerous biological properties of pyrrole derivatives, in particular antimicrobial, antibacterial, antifungal, antimalarial, anticancer activities, etc. Therefore, pyrroles serve as building blocks in the creation of potential pharmaceuticals and also serve as the basis for the synthesis of boradipyrromethene dyes. One of the most well-known approaches to the synthesis of pyrroles is the reaction between nitroolefins, 1,3-dicarbonyl compounds, and amines, also known as the Grob-Camenisch reaction. This review is devoted to the historical chronology from the discovery of this transformation dating back to 1950s to the present, and covers the development of various modifications of the above reaction in the synthesis of pyrroles.
Authors
- Yuriy P. Kovtun (ORCID: https://orcid.org/0000-0002-2673-5342)
- Andrii H. Hotynchan (ORCID: https://orcid.org/0000-0002-1569-8590)
- Olena M. Kovtun
Institutions
- National Academy of Sciences of Ukraine (UA)
- Dragomanov Ukrainian State University (UA)
- Institute of Organic Chemistry (UA)
Publication Details
- Journal
- Journal of organic and pharmaceutical chemistry
- Published
- 2025-06-11
- DOI
- https://doi.org/10.24959/ophcj.25.323775
- Primary Topic
- Synthesis and Characterization of Pyrroles
- Type
- article
- Field-Weighted Citation Impact
- 0.00