Well Defined Phosphine Free Ni‐Catalyzed Dehydrogenation of Secondary Alcohols for the Synthesis of Ketones and Ketazines

In this work, we unveil a novel synthesis of bench stable Ni (II) complexes supported by tetradentate Schiff-base ligands and the complexes were devoid of any phosphine or phosphine-based ligand. These Ni-complexes were successfully applied for the dehydrogenation of secondary alcohols for ketone and ketazine syntheses. Secondary alcohols with different functional groups were well tolerated during catalytic cycle. Moreover, we successfully extended this protocol for the synthesis of biologically significant ketones and ketazines. On the basis of various control experiments, probable reaction pathway was proposed, and an acceptorless alcohol dehydrogenation mechanism was suggested.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2024-10-04
DOI
https://doi.org/10.1002/asia.202400818
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.32
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article

Well Defined Phosphine Free Ni‐Catalyzed Dehydrogenation of Secondary Alcohols for the Synthesis of Ketones and Ketazines

Ankur Maji, Sheela Kumari, Kaushik Ghosh, Ovender Singh et al.
2 citations
Chemistry - An Asian Journal
Asymmetric Hydrogenation and Catalysis
0.32
article

Well Defined Phosphine Free Ni‐Catalyzed Dehydrogenation of Secondary Alcohols for the Synthesis of Ketones and Ketazines

Ankur Maji, Sheela Kumari, Kaushik Ghosh, Ovender Singh, Keshav Sharma
article en
2 citations

Abstract

In this work, we unveil a novel synthesis of bench stable Ni (II) complexes supported by tetradentate Schiff-base ligands and the complexes were devoid of any phosphine or phosphine-based ligand. These Ni-complexes were successfully applied for the dehydrogenation of secondary alcohols for ketone and ketazine syntheses. Secondary alcohols with different functional groups were well tolerated during catalytic cycle. Moreover, we successfully extended this protocol for the synthesis of biologically significant ketones and ketazines. On the basis of various control experiments, probable reaction pathway was proposed, and an acceptorless alcohol dehydrogenation mechanism was suggested.

Chemistry - An Asian JournalVol. 19(24)
Indian Institute of Technology Roorkee (IN)
Clean water and sanitation
Openalex Percentile: Top 49%
Asymmetric Hydrogenation and Catalysis
0.32
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