75279-53-7Relevant articles and documents
Rapid and Simple Access to α-(Hetero)arylacetonitriles from Gem-Difluoroalkenes
Hu, Dandan,Liu, Jiayue,Ren, Hongjun,Song, Jinyu,Zhang, Jun-Qi,Zhu, Guorong
supporting information, p. 786 - 790 (2022/01/28)
A scalable cyanation of gem-difluoroalkenes to (hetero)arylacetonitrile derivatives was developed. This strategy features mild reaction conditions, excellent yields, wide substrate scope, and broad functional group tolerance. Significantly, in this reacti
PYRIDINE-2-CARBOXAMIDES AS NEMATOCIDES
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Page/Page column 41, (2015/02/02)
Compounds of the formula (I), in which the substituents are as defined in claim 1, are suitable for use as nematicides.
ELECTRFLUORATION EN POSITION BENZYLIQUE DANS LE SULFOLANE
Laurent, Eliane,Marquet, Bernard,Tardivel, Robert
, p. 115 - 126 (2007/10/02)
The use of sulfolane as a solvent instead of acetonitrile in the electrofluorination of benzylic derivatives 1, (R=H, Cl) gives greater yields of benzylic fluorides 2, since the formation of acetamide byproducts 4 is prevented.However, the parallel fluorination of the aromatic nucleus is not avoided under these conditions.