Bis-guanidinate magnesium amide-catalyzed hydroboration of nitriles and isocyanides <i>via</i> a substrate-assisted pathway

Magnesium catalysis : A bis-guanidinate magnesium amido complex enables the first example of a substrate-assisted catalytic dihydroboration of nitriles and isocyanides, with the isolation of key intermediates and elucidation of catalytic cycles.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-10-24
DOI
https://doi.org/10.1039/d5qo01184a
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Bis-guanidinate magnesium amide-catalyzed hydroboration of nitriles and isocyanides via a substrate-assisted pathway

Organic Chemistry Frontiers
Organoboron and organosilicon chemistry
article

Bis-guanidinate magnesium amide-catalyzed hydroboration of nitriles and isocyanides via a substrate-assisted pathway

article en

Abstract

Magnesium catalysis : A bis-guanidinate magnesium amido complex enables the first example of a substrate-assisted catalytic dihydroboration of nitriles and isocyanides, with the isolation of key intermediates and elucidation of catalytic cycles.

Organic Chemistry FrontiersVol. 13(2)
National Institute of Science Education and Research (IN)
National Institute of Science Education and Research, Homi Bhabha National Institute, Science and Engineering Research Board
Openalex Percentile: Top 45%
Organoboron and organosilicon chemistry
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Bis-guanidinate magnesium amide-catalyzed hydroboration of nitriles and isocyanides <i>via</i> a substrate-assisted pathway · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS