Divergent Iron-Catalyzed Olefin Cyclization for Saturated <i>N</i> -Heterocycles Syntheses

Saturated N-heterocycles are important motifs in pharmaceuticals, agrochemicals, and materials. While many catalytic methods can cyclize an intramolecular N-containing substrate into one specific <i>N</i>-heterocycle, the regio-complementary cyclization process is often difficult to achieve. Herein, we report the development of two simple iron catalytic protocols enabling divergent cyclization of a common precursor into distinct N-heterocyclic motifs, including pyrrolidines, piperidines, and azepanes.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-12-22
DOI
https://doi.org/10.1021/acs.joc.5c02681
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Divergent Iron-Catalyzed Olefin Cyclization for Saturated N -Heterocycles Syntheses

Alex M. Nguyen, Navdeep Kaur, Kim T. Huynh, Wei Li et al.
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

Divergent Iron-Catalyzed Olefin Cyclization for Saturated N -Heterocycles Syntheses

Alex M. Nguyen, Navdeep Kaur, Kim T. Huynh, Wei Li, Pritha Dutta, Kristi Shrestha, Glenn M. Chambers
article en

Abstract

Saturated N-heterocycles are important motifs in pharmaceuticals, agrochemicals, and materials. While many catalytic methods can cyclize an intramolecular N-containing substrate into one specific <i>N</i>-heterocycle, the regio-complementary cyclization process is often difficult to achieve. Herein, we report the development of two simple iron catalytic protocols enabling divergent cyclization of a common precursor into distinct N-heterocyclic motifs, including pyrrolidines, piperidines, and azepanes.

The Journal of Organic ChemistryVol. 91(1)
University of Toledo (US)
Openalex Percentile: Top 34%
Catalytic C–H Functionalization Methods
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