Metal‐Ligand Cooperative Cobalt (II) Catalysts for Synthesis of Triaryl Pyrazolines and Bis(indolyl)methanes via Alcohol Dehydrogenation

In this study, the catalytic activity of cobalt complexes (Cat‐1 and Cat‐2) based on tetrazine ligand was examined for the synthesis of 1,3,5‐triaryl‐substituted 2‐pyrazolines via a multicomponent strategy and the coupling of alcohols with indoles to produce bis(indolyl)methanes (BIMs). The method utilizes alcohols as green alkylating agents under dehydrogenative conditions, offering a sustainable and atom‐economical approach. The methodology exhibits a wide substrate scope of 82 examples showing excellent functional group tolerance, including 13 bioactive compounds. Control experiments studies combined with the detection of key intermediates through UV–vis, fourier‐transform infrared spectroscopy, and high resolution mass spectrometry (HRMS) suggested the involvement of metal‐ligand cooperation in the plausible reaction pathway.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-15
DOI
https://doi.org/10.1002/ejoc.202501172
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
0.00

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article

Metal‐Ligand Cooperative Cobalt (II) Catalysts for Synthesis of Triaryl Pyrazolines and Bis(indolyl)methanes via Alcohol Dehydrogenation

Sheela Kumari, Kaushik Ghosh, Prashant Kukreti, Rahul Chauhan
European Journal of Organic Chemistry
Synthesis of Indole Derivatives
article

Metal‐Ligand Cooperative Cobalt (II) Catalysts for Synthesis of Triaryl Pyrazolines and Bis(indolyl)methanes via Alcohol Dehydrogenation

Sheela Kumari, Kaushik Ghosh, Prashant Kukreti, Rahul Chauhan
article en

Abstract

In this study, the catalytic activity of cobalt complexes (Cat‐1 and Cat‐2) based on tetrazine ligand was examined for the synthesis of 1,3,5‐triaryl‐substituted 2‐pyrazolines via a multicomponent strategy and the coupling of alcohols with indoles to produce bis(indolyl)methanes (BIMs). The method utilizes alcohols as green alkylating agents under dehydrogenative conditions, offering a sustainable and atom‐economical approach. The methodology exhibits a wide substrate scope of 82 examples showing excellent functional group tolerance, including 13 bioactive compounds. Control experiments studies combined with the detection of key intermediates through UV–vis, fourier‐transform infrared spectroscopy, and high resolution mass spectrometry (HRMS) suggested the involvement of metal‐ligand cooperation in the plausible reaction pathway.

European Journal of Organic Chemistry
Indian Institute of Technology Roorkee (IN)
Council of Scientific and Industrial Research, India
Openalex Percentile: Top 18%
Synthesis of Indole Derivatives
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