Multifunctional PNN-Ni<sup>II</sup> pincer catalyst for C–C and C–N bond formation <i>via</i> alkylation, cross-coupling, and hydroamination reactions

A new Ni II pincer complex [NiCl{(PNN)-κ 3 - P,N,N }] catalyses α-alkylation of ketones, N -alkylation of anilines, Suzuki couplings, and anti-Markovnikov hydroamination of styrenes with 0.5–1 mol% loading, affording up to 99% yield under mild conditions.

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Publication Details

Journal
Catalysis Science & Technology
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cy00718f
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.07
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article

Multifunctional PNN-NiII pincer catalyst for C–C and C–N bond formation via alkylation, cross-coupling, and hydroamination reactions

Maravanji S. Balakrishna, Gazal Sabharwal, Khilesh C. Dwivedi
2 citations
Catalysis Science & Technology
Asymmetric Hydrogenation and Catalysis
1.07
article

Multifunctional PNN-NiII pincer catalyst for C–C and C–N bond formation via alkylation, cross-coupling, and hydroamination reactions

Maravanji S. Balakrishna, Gazal Sabharwal, Khilesh C. Dwivedi
article en
2 citations

Abstract

A new Ni II pincer complex [NiCl{(PNN)-κ 3 - P,N,N }] catalyses α-alkylation of ketones, N -alkylation of anilines, Suzuki couplings, and anti-Markovnikov hydroamination of styrenes with 0.5–1 mol% loading, affording up to 99% yield under mild conditions.

Catalysis Science & TechnologyVol. 15(18)
Indian Institute of Technology Bombay (IN)
Openalex Percentile: Top 22%
Asymmetric Hydrogenation and Catalysis
1.07
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