Mechanochemical synthesis of aromatic ketones: pyrylium tetrafluoroborate mediated deaminative arylation of amides.
Satenik MkrtchyanOleksandr ShalimovMichael G GarciaJiří ZapletalViktor O IaroshenkoPublished in: Chemical science (2024)
A new method has been introduced that is able to tackle the complexities of N-C(O) activation in amide moieties through utilization of pyrylium tetrafluoroborate in a mechanochemical setting, where amide bonds undergo activation and subsequent conversion to biaryl ketones. Due to the employment of a mechanochemical setting, the reaction conforms to green chemistry principles, offering an environmentally friendly approach to traditional amide derivatization techniques that rely on transition metals to achieve further functionalization.
Keyphrases
- ms ms
- liquid chromatography tandem mass spectrometry
- high performance liquid chromatography
- human health
- tandem mass spectrometry
- risk assessment
- health risk
- mental health
- amino acid
- liquid chromatography
- mental illness
- drug discovery
- high resolution
- heavy metals
- electron transfer
- ultra high performance liquid chromatography
- transition metal