Trapping <i>in situ</i> generated CF<sub>3</sub>-nitrile imines with maleimides under solvent-free mechanochemical conditions

A series of trifluoromethylated pyrrolo[3,4- c ]pyrazoles were obtained via mechanochemical (3 + 2)-cycloaddition of in situ generated trifluoroacetonitrile imines with maleimide and its N -aliphatic/aromatic analogues.

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Publication Details

Journal
RSC Mechanochemistry
Published
2024-11-07
DOI
https://doi.org/10.1039/d4mr00075g
Citations
4
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.83

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article

Trapping in situ generated CF3-nitrile imines with maleimides under solvent-free mechanochemical conditions

Szymon Jarzyński, Greta Utecht‐Jarzyńska, Marcin Jasiński
4 citations
RSC Mechanochemistry
Fluorine in Organic Chemistry
0.83
article

Trapping in situ generated CF3-nitrile imines with maleimides under solvent-free mechanochemical conditions

Szymon Jarzyński, Greta Utecht‐Jarzyńska, Marcin Jasiński
article en
4 citations

Abstract

A series of trifluoromethylated pyrrolo[3,4- c ]pyrazoles were obtained via mechanochemical (3 + 2)-cycloaddition of in situ generated trifluoroacetonitrile imines with maleimide and its N -aliphatic/aromatic analogues.

RSC MechanochemistryVol. 2(1)
University of Łódź (PL)
Uniwersytet Łódzki
Openalex Percentile: Top 30%
Fluorine in Organic Chemistry
0.83
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