Trifluoromethylation of N-Benzoylhydrazones
The Journal of Organic Chemistry2008Vol. 73(14), pp. 5643–5646
Citations Over TimeTop 10% of 2008 papers
Alexander D. Dilman, Dmitry E. Arkhipov, Vitalij V. Levin, Pavel A. Belyakov, Аlexander А. Korlyukov, Марина И. Стручкова, Vladimir A. Tartakovsky
Abstract
A method for the nucleophilic trifluoromethylation of N-benzoylhydrazones using Me3SiCF3/AcONa has been described. The CN bond of the hydrazones is activated by difluoroboron group, which is introduced by means of boron trifluoride and allylsilane.
Related Papers
- → Recent advances in trifluoromethylation of organic compounds using Umemoto's reagents(2014)205 cited
- → Progress in copper-catalyzed trifluoromethylation(2018)99 cited
- → Copper-catalyzed trifluoromethylation of arylsulfinate salts using an electrophilic trifluoromethylation reagent(2013)32 cited
- → Copper-Catalyzed Trifluoromethylation of Alkoxypyridine Derivatives(2020)3 cited
- → ChemInform Abstract: Recent Advances in Trifluoromethylation of Organic Compounds Using Umemoto′s Reagents(2014)