Reversibility of the transfer hydrogenation reaction was found to be low under these reaction circumstances.
📌 3 Key Takeaways
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Objective & Hypothesis:Since the obtained chiral alcohols are rather useful as well as biologically active compounds, reduction of ketones to their respective alcohols is a crucial topic in synthetic chemistry.
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Key Findings & Data:Thus, a new phosphinite ligand was synthesized by the interaction of cationic species N-vinyl imidazolium (1) with PCy2Cl.
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Conclusion & Impact:Reversibility of the transfer hydrogenation reaction was found to be low under these reaction circumstances.
Since the obtained chiral alcohols are rather useful as well as biologically active compounds, reduction of ketones to their respective alcohols is a crucial topic in synthetic chemistry. Thus, a new phosphinite ligand was synthesized by the interaction of cationic species N-vinyl imidazolium (1) with PCy2Cl. This phosphinite ligand in combination with [Ru(η6-p-cymene)(µ-Cl)Cl]2 and Ir(η5-C5Me5)(μ-Cl)Cl]2 gave active catalytic systems for transfer hydrogenation reaction. Under optimum circumstances, ruthenium complex (3) showed rather high conversion reduction reaction of acetophenone. Reversibility of the transfer hydrogenation reaction was found to be low under these reaction circumstances.
IŞIK, U., MERİÇ, N., AYDEMİR, M. (2022). NOVEL MONONUCLEAR METAL-PHOSPHINITE COMPOUNDS AND CATALYTIC PERFORMANCE IN TRANSFER HYDROGENATION OF KETONES. Middle East Journal of Science, Cilt: 8 - Sayı: 1, 1–15. https://ajindex.com/articles/580415
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