ABNO‐Catalyzed Oxidative Dehydrogenation of <i>N</i> ‐Heterocycles in the Synthesis of <i>N</i> ‐Heteroarenes

ABSTRACT We report a method for catalyzing the oxidative dehydrogenation of tetrahydroquinoline and indoline derivatives under metal‐free conditions. With 9‐azabicyclo[3.3.1]nonane N ‐oxyl (ABNO) as the catalyst in the presence of potassium tert‐butoxide ( t BuOK), this approach facilitates the efficient oxidative dehydrogenation of partially saturated N ‐heterocyclic arylamines to their aromatic counterparts, offering an alternative approach for N ‐heterocycle synthesis.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-11-08
DOI
https://doi.org/10.1002/ajoc.70256
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

ABNO‐Catalyzed Oxidative Dehydrogenation of N ‐Heterocycles in the Synthesis of N ‐Heteroarenes

Jianwei Han, Haoyang Wang, H. Yang, Hui Han et al.
Asian Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

ABNO‐Catalyzed Oxidative Dehydrogenation of N ‐Heterocycles in the Synthesis of N ‐Heteroarenes

Jianwei Han, Haoyang Wang, H. Yang, Hui Han, Limin Wang
article en

Abstract

ABSTRACT We report a method for catalyzing the oxidative dehydrogenation of tetrahydroquinoline and indoline derivatives under metal‐free conditions. With 9‐azabicyclo[3.3.1]nonane N ‐oxyl (ABNO) as the catalyst in the presence of potassium tert‐butoxide ( t BuOK), this approach facilitates the efficient oxidative dehydrogenation of partially saturated N ‐heterocyclic arylamines to their aromatic counterparts, offering an alternative approach for N ‐heterocycle synthesis.

Asian Journal of Organic ChemistryVol. 15(1)
East China University of Science and Technology (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 75%
Catalytic C–H Functionalization Methods
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