Copper-Catalyzed Direct Trifluoromethylthiolation of Benzylic C–H Bonds via Nondirected Oxidative C(sp3)–H Activation
Organic Letters2014Vol. 16(12), pp. 3372–3375
Citations Over TimeTop 1% of 2014 papers
Abstract
A copper-catalyzed trifluoromethylthiolation of benzylic sp(3) C-H bonds was developed via nondirected oxidative C-H activation using readily prepared and stable AgSCF3. This reaction provides a novel and straightforward method for the preparation of various benzyl trifluoromethyl sulfides.
Related Papers
- → Enhanced catalytic activity of Pt/Al2O3 on the CH4 SCR(2011)24 cited
- → Catalytic reduction of N2O with CH4 over FeAlPO-5 catalyst(2008)15 cited
- → Determining influence of catalyst-reductant morphology on two different mechanisms of SCR by MOFs(2021)3 cited
- → Catalytic activity of H3PMo12−XWXO40 and H6P2MO18−XWXO62 heteropolyacid (HPA) catalysis in the direct preparation of dichloropropanol (DCP) from glycerol(2008)9 cited
- → ИСПОЛЬЗОВAНИЕ ПОТЕНЦИAЛA СОЦИAЛЬНЫХ ПAРТНЕРОВ В ПОДГОТОВКЕ БУДУЩИХ ПЕДAГОГОВ(2024)