Web10 jan. 2024 · This paper presents a straightforward and quantitative strategy for the preparation of valuable AgOCF3 at room temperature and showcases its performance in trifluoromethoxylations or as reservoir for O=CF2 . The development of innovative fluorination strategies is greatly dependent also on the availability, safety and … Web9 dec. 2016 · Reported herein is the one-pot synthesis of trifluoromethylated amines at room temperature using the bench-stable (Me 4 N)SCF 3 reagent and AgF. The method is …
Recent Advances and Uses of (Me 4 N)XCF 3 (X=S, Se) in the …
Web1 dec. 2024 · Using experimental reactivity tests, ReactIR and computational techniques, we herein showcase that the solid (Me4N)SCF3 functions as a safe reservoir for S=CF2. A … Web2 jan. 2024 · Efficient Synthesis of Trifluoromethyl Amines through a Formal Umpolung Strategy from the Bench-Stable Precursor (Me 4 N)SCF 3 Angew Chem Int Ed Engl. 2024 Jan 2;56 (1):221-224. doi: 10.1002/anie.201609480. Epub 2016 Dec 9. Authors Thomas Scattolin 1 , Kristina Deckers 1 , Franziska Schoenebeck 1 Affiliation labbled ignious thin section
Tetramethylammonium Trifluoromethanethiolate (Me4N)SCF3 - Scattolin
Web(Me 4 N)SCF 3 - From the Use in Metal-Catalyzed Processes to the Synthesis of Trifluoromethylated Amines (N-CF 3) Thomas Scattolin, Kristina Deckers, Franziska … Web12 okt. 2024 · Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me4N)SCF3. A convenient, highly efficient, and selective … Web12 jan. 2024 · Using experimental reactivity tests, ReactIR and computational techniques, we herein showcase that the solid (Me 4 N)SCF 3 functions as a safe reservoir for S=CF 2 . A key feature is that the reactive electrophile is not simply released over time, but instead is liberated under activation with a protic nucleophile. projects bathroom