Mind the gap! Steric-driven reductive desymmetrisation of malononitriles

<h2>Abstract</h2> Huang and coworkers recently demonstrated that a cobalt(I)-hydride complex, ligated with a finely tuned chiral bisoxazoline ligand, can selectively reduce disubstituted malononitriles by discriminating between enantiotopic nitrile groups. This reductive desymmetrisation strategy utilises the bulk industrial feedstock malononitrile to access nitrogen-rich enantioenriched products.

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Publication Details

Journal
Trends in Chemistry
Published
2024-12-26
DOI
https://doi.org/10.1016/j.trechm.2024.12.002
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Mind the gap! Steric-driven reductive desymmetrisation of malononitriles

Reece Hoogesteger, Craig P. Johnston, Cara Philipson
Trends in Chemistry
Asymmetric Synthesis and Catalysis
article

Mind the gap! Steric-driven reductive desymmetrisation of malononitriles

Reece Hoogesteger, Craig P. Johnston, Cara Philipson
article en

Abstract

<h2>Abstract</h2> Huang and coworkers recently demonstrated that a cobalt(I)-hydride complex, ligated with a finely tuned chiral bisoxazoline ligand, can selectively reduce disubstituted malononitriles by discriminating between enantiotopic nitrile groups. This reductive desymmetrisation strategy utilises the bulk industrial feedstock malononitrile to access nitrogen-rich enantioenriched products.

Trends in ChemistryVol. 7(2)
University of St Andrews (GB)
Royal Society, Syngenta International, Engineering and Physical Sciences Research Council
Zero hunger
Openalex Percentile: Top 82%
Asymmetric Synthesis and Catalysis
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