Issue 7, 2024

NNN manganese complex-catalyzed α-alkylation of methyl ketones using alcohols: an experimental and computational study

Abstract

We present here a phosphine-free, quinoline-based pincer Mn catalyst for α-alkylation of methyl ketones using primary alcohols as alkyl surrogates. The C–C bond formation reaction proceeds via a hydrogen auto-transfer methodology. The sole by-product formed is water, rendering the protocol atom efficient. Electronic structure theory studies corroborated the proposed mechanism.

Graphical abstract: NNN manganese complex-catalyzed α-alkylation of methyl ketones using alcohols: an experimental and computational study

Supplementary files

Article information

Article type
Paper
Submitted
22 Dec 2023
Accepted
08 Jan 2024
First published
09 Jan 2024

Dalton Trans., 2024,53, 3236-3243

NNN manganese complex-catalyzed α-alkylation of methyl ketones using alcohols: an experimental and computational study

S. Jalwal, A. Regina, V. Atreya, M. Paranjothy and S. Chakraborty, Dalton Trans., 2024, 53, 3236 DOI: 10.1039/D3DT04321E

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