Catalytic Hydroboration of Ketones Using Mn(CO) <sub>5</sub> Br and Mn <sub>2</sub> (CO) <sub>10</sub>

The commercially available and easy‐to‐handle manganese complexes Mn(CO) 5 Br and Mn 2 (CO) 10 effectively catalyze the hydroboration of ketones under mild conditions, yielding secondary alcohols after hydrolysis. These simple catalysts exhibit broad tolerance to different functional groups including esters, halides, and nitroarenes. Moreover, the reaction proceeds with high chemoselectivity toward CO bonds in the presence of esters, nitriles, nitro groups, or double CC bond. The proposed procedure enables fast, efficient synthesis of O‐borylated products, which are easily hydrolyzed in a one‐pot manner to various aryl and alkyl alcohols (even unsaturated ones) in excellent yields. Thus, the developed procedure compares favorably with other Mn catalytic systems, which require lengthy preparation, the application of structurally and electronically advanced ligands, and oxygen‐ and moisture‐free conditions.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-08-28
DOI
https://doi.org/10.1002/adsc.70092
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

Catalytic Hydroboration of Ketones Using Mn(CO) 5 Br and Mn 2 (CO) 10

Marc‐Etienne Moret, Jakub Szyling, Jędrzej Walkowiak, Subhabrata De et al.
Advanced Synthesis & Catalysis
Asymmetric Hydrogenation and Catalysis
article

Catalytic Hydroboration of Ketones Using Mn(CO) 5 Br and Mn 2 (CO) 10

Marc‐Etienne Moret, Jakub Szyling, Jędrzej Walkowiak, Subhabrata De, Barbara Krupa, Katarina Ležaić, Mateusz Nowicki, Aleksandra Szymańska
article en

Abstract

The commercially available and easy‐to‐handle manganese complexes Mn(CO) 5 Br and Mn 2 (CO) 10 effectively catalyze the hydroboration of ketones under mild conditions, yielding secondary alcohols after hydrolysis. These simple catalysts exhibit broad tolerance to different functional groups including esters, halides, and nitroarenes. Moreover, the reaction proceeds with high chemoselectivity toward CO bonds in the presence of esters, nitriles, nitro groups, or double CC bond. The proposed procedure enables fast, efficient synthesis of O‐borylated products, which are easily hydrolyzed in a one‐pot manner to various aryl and alkyl alcohols (even unsaturated ones) in excellent yields. Thus, the developed procedure compares favorably with other Mn catalytic systems, which require lengthy preparation, the application of structurally and electronically advanced ligands, and oxygen‐ and moisture‐free conditions.

Advanced Synthesis & CatalysisVol. 367(17)
Utrecht University (NL), Adam Mickiewicz University in Poznań (PL)
Openalex Percentile: Top 82%
Asymmetric Hydrogenation and Catalysis
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