Sustainable Synthesis of <i>N</i> -Substituted Pyrroles via Fe-Catalyzed One-Pot Multicomponent Reaction

Herein, we present a one-pot strategy for synthesizing <i>N</i>-substituted pyrroles from readily accessible feedstocks, such as alcohols, diols, and amines, catalyzed by a well-defined Fe(II)-catalyst featuring a redox-active azo-aromatic-1,10-phenanthroline-based ligand. Compared to existing approaches, this protocol enables access to diverse pyrrole derivatives, including penta-substituted pyrroles and complex polycyclic frameworks in good yields with improved atom economy and broad functional-group tolerance.

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Publication Details

Journal
Organic Letters
Published
2026-03-16
DOI
https://doi.org/10.1021/acs.orglett.6c00539
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
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article

Sustainable Synthesis of N -Substituted Pyrroles via Fe-Catalyzed One-Pot Multicomponent Reaction

Santana Chakraborty, Nanda Dulal Paul, Arijit Singha Mohapatra
Organic Letters
Synthesis and Characterization of Pyrroles
article

Sustainable Synthesis of N -Substituted Pyrroles via Fe-Catalyzed One-Pot Multicomponent Reaction

Santana Chakraborty, Nanda Dulal Paul, Arijit Singha Mohapatra
article en

Abstract

Herein, we present a one-pot strategy for synthesizing <i>N</i>-substituted pyrroles from readily accessible feedstocks, such as alcohols, diols, and amines, catalyzed by a well-defined Fe(II)-catalyst featuring a redox-active azo-aromatic-1,10-phenanthroline-based ligand. Compared to existing approaches, this protocol enables access to diverse pyrrole derivatives, including penta-substituted pyrroles and complex polycyclic frameworks in good yields with improved atom economy and broad functional-group tolerance.

Organic LettersVol. 28(12)
Institute of Engineering Science (RU)
Industry, innovation and infrastructure, Responsible consumption and production
Openalex Percentile: Top 17%
Synthesis and Characterization of Pyrroles
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