Magnesium bromide‐catalyzed solvent‐free hydroboration of imines: An eco‐friendly approach to amines

Abstract Over the past decade, significant progress has been made in the area of catalytic hydroboration reactions, wherein a variety of catalytic systems have been reported. To develop green and sustainable methods, an environmental friendly and cost‐effective alternatives to traditional expensive, toxic metal catalysts are required. In this study, we report a simple and high‐yielding magnesium salt (MgBr 2 )‐catalyzed hydroboration reaction of imines with pinacolborane (HBpin). The chemoselective hydroboration of imines over ester, amide, nitrile, alkene, and alkyne functional groups was also evaluated. In addition, gram scale preparation, one‐pot N–C coupling reactions, and density functional theory mechanistic studies were performed.

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Publication Details

Journal
Bulletin of the Korean Chemical Society
Published
2026-02-01
DOI
https://doi.org/10.1002/bkcs.70106
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Magnesium bromide‐catalyzed solvent‐free hydroboration of imines: An eco‐friendly approach to amines

Ji Eun Seok, Duk Keun An, Ji Hye Lee, Ashok Kumar Jaladi et al.
Bulletin of the Korean Chemical Society
Organoboron and organosilicon chemistry
article

Magnesium bromide‐catalyzed solvent‐free hydroboration of imines: An eco‐friendly approach to amines

Ji Eun Seok, Duk Keun An, Ji Hye Lee, Ashok Kumar Jaladi, Kyung Hwa Ryu
article en

Abstract

Abstract Over the past decade, significant progress has been made in the area of catalytic hydroboration reactions, wherein a variety of catalytic systems have been reported. To develop green and sustainable methods, an environmental friendly and cost‐effective alternatives to traditional expensive, toxic metal catalysts are required. In this study, we report a simple and high‐yielding magnesium salt (MgBr 2 )‐catalyzed hydroboration reaction of imines with pinacolborane (HBpin). The chemoselective hydroboration of imines over ester, amide, nitrile, alkene, and alkyne functional groups was also evaluated. In addition, gram scale preparation, one‐pot N–C coupling reactions, and density functional theory mechanistic studies were performed.

Bulletin of the Korean Chemical SocietyVol. 47(2)
Kangwon National University (KR)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Responsible consumption and production, Life in Land
Openalex Percentile: Top 66%
Organoboron and organosilicon chemistry
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