دورية أكاديمية

Selective Access to Functional Fluoroenones via Palladium-Catalyzed Selenofluoroalkylacylation of Terminal Alkynes

التفاصيل البيبلوغرافية
العنوان: Selective Access to Functional Fluoroenones via Palladium-Catalyzed Selenofluoroalkylacylation of Terminal Alkynes
المؤلفون: Ya Li, Dian Dong, Lintong Chen, Hongxuan Du, Cong Zhao, Xiaoyan Bai, Lu Chen, Yibiao Li, Xianghua Zeng, Pierre H. Dixneuf, Min Zhang
سنة النشر: 1753
مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Inorganic Chemistry, Infectious Diseases, Virology, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, polar crossover process, mechanistic studies reveal, alkyl disubstituted enones, reaction proceeds via, widely studied, terminal alkynes, selective access, oxidative radical, novel palladium, mild conditions, medicinal chemistry, materials science, important motif, diorganyl diselenides, catalyzed selenofluoroalkylacylation, also suitable, afford β
الوصف: The trifluoromethylacyl group (−COCF 3 ) is an important motif and widely studied in catalysis, medicinal chemistry, and materials science. Herein, a novel palladium-catalyzed selenofluoroalkylacylation of terminal alkynes with commercially available fluoroalkyl anhydride and diorganyl diselenides to afford β-seleno and aryl/alkyl disubstituted enones under mild conditions is disclosed. In addition, selenodifluoroacetylations and selenoperfluoroacetylations are also suitable for this reaction. Mechanistic studies reveal that this reaction proceeds via an oxidative radical-polar crossover process.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
العلاقة: https://figshare.com/articles/journal_contribution/Selective_Access_to_Functional_Fluoroenones_via_Palladium-Catalyzed_Selenofluoroalkylacylation_of_Terminal_Alkynes/25028893Test
DOI: 10.1021/acs.orglett.3c04191.s001
الإتاحة: https://doi.org/10.1021/acs.orglett.3c04191.s001Test
https://figshare.com/articles/journal_contribution/Selective_Access_to_Functional_Fluoroenones_via_Palladium-Catalyzed_Selenofluoroalkylacylation_of_Terminal_Alkynes/25028893Test
حقوق: CC BY-NC 4.0
رقم الانضمام: edsbas.23514E84
قاعدة البيانات: BASE