Persulfate-promoted radical cascade trifluoromethylthiolation and cyclization of 3-alkyl-1-(2-(alkynyl)phenyl)indoles with AgSCF were investigated. This protocol provides a novel route to CFS-substituted indolo[1,2-]quinoline-7-carbaldehydes and CFS-substituted indolo[1,2-]quinoline-7-methanone derivatives via the formation of the C-SCF bond and C-C bond and benzylic carbon oxidation in a single step. This reaction can accommodate a broad range of functional groups. The single-crystal X-ray diffraction data confirm the chemical structure of the product. A scale-up experiment and radical inhibition experiments were operated in the reaction system. Photophysical properties of some selected 5-((trifluoromethyl)thio)indolo[1,2-]quinoline-7-carbaldehydes were studied by UV-visible and fluorescence spectroscopy.
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http://dx.doi.org/10.1021/acs.joc.2c03045 | DOI Listing |
Org Biomol Chem
December 2024
College of Chemistry, Zhengzhou University, Zhengzhou 450001, People's Republic of China.
A silver-mediated cascade trifluoromethylthiolation/cyclization of unactivated alkenes has been investigated. This strategy employs AgSCF as the trifluoromethylthiolating reagent to obtain a variety of useful trifluoromethylthiolated tricyclic imidazol derivatives in reasonable yields. Preliminary mechanistic studies indicate that the present reaction takes place a radical process.
View Article and Find Full Text PDFJ Org Chem
September 2024
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, Shanghai University of Electric Power, Shanghai 200090, China.
An environmentally friendly electrochemical strategy for the synthesis of SCF-containing oxindoles was developed. This electrochemical transformation was accomplished through a cascade trifluoromethylthiolation/cyclization of -acrylamides with AgSCF, obviating the requirement for external oxidants. A variety of functional groups were well tolerated in this transformation.
View Article and Find Full Text PDFOrg Lett
June 2023
College of Chemistry and Chemical Engineering, Yantai University, Yantai, 264005, P. R. China.
A novel radical cascade trifluoromethylthiolation/cyclization of dienes (-alkyl-2-(1-phenylvinyl)aniline derivatives) with AgSCF has been developed. This approach provides simple and efficient access to a wide range of SCF-containing medium-sized rings (7/8/9-membered heterocycles). Preliminary mechanistic studies suggest that the reaction is realized through a silver-assisted radical cascade cyclization process.
View Article and Find Full Text PDFOrg Lett
May 2023
Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China.
The BnSR (R = CFH or CF)/CPBA/TfO system was found to be an effective multicomponent reagent system for the one-pot synthesis of di/trifluoromethylthiolated heterocycles from alkynes. The reaction was postulated to proceed via a cascade sequence involving the oxidation of BnSR by CPBA, activation of the in situ-generated sulfoxide by TfO, and intramolecular cyclization/fluoromethylthiolation of the alkyne substrates enabled by the formed electrophilic sulfonium salt to give di/trifluoromethylthiolated heterocycles.
View Article and Find Full Text PDFJ Org Chem
May 2023
Department of Chemistry and Center of Excellence for Innovation in Chemistry (PERCH-CIC), Faculty of Science, Mahidol University, Rama VI Road, Bangkok 10400, Thailand.
Persulfate-promoted radical cascade trifluoromethylthiolation and cyclization of 3-alkyl-1-(2-(alkynyl)phenyl)indoles with AgSCF were investigated. This protocol provides a novel route to CFS-substituted indolo[1,2-]quinoline-7-carbaldehydes and CFS-substituted indolo[1,2-]quinoline-7-methanone derivatives via the formation of the C-SCF bond and C-C bond and benzylic carbon oxidation in a single step. This reaction can accommodate a broad range of functional groups.
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