Academic Journal

FluoroFusion: NHC-Catalyzed Nucleophilic Aromatic Substitution Reaction Unveils Functional Perfluorinated Diarylmethanones

التفاصيل البيبلوغرافية
العنوان: FluoroFusion: NHC-Catalyzed Nucleophilic Aromatic Substitution Reaction Unveils Functional Perfluorinated Diarylmethanones
المؤلفون: Chan, Cheng-Lin, Lee, Shao-Chi, Lin, Pei-Shan, Tapales, Radyn Vanessa Phaz P., Li, Jia-Syuan, Lai, Chun-An, Lee, Jyh-Tsung, Li, Chien-Hung, Liao, Hsuan-Hung
المساهمون: KAUST Catalysis Center (KCC), Physical Science and Engineering (PSE) Division, Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.), Department of International Ph.D. Program for Science, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.), Department of Chemistry, National Chung Hsing University, Taichung 402202, Taiwan (R.O.C.), Department of Applied and Medicinal Chemistry, Kaohsiung Medical University, Kaohsiung 807378, Taiwan (R.O.C.)
بيانات النشر: American Chemical Society (ACS)
سنة النشر: 2024
المجموعة: King Abdullah University of Science and Technology: KAUST Repository
الوصف: A mild, facile, and metal-free approach via the N-heterocyclic carbene-catalyzed SNAr reaction between aryl aldehydes with perfluoroarenes to obtain the coveted functional perfluorinated diarylmethanones is disclosed. This method accommodates a diverse substrate range and exhibits notable tolerance toward various functional groups. Our success in modifying biologically relevant molecules, crafting a fully fluorinated bioisosteric analogue of drug candidate D1, and highlighting the potential of these ketones as valuable electrolyte additives for lithium-ion batteries (LIBs) underscores the versatility of our methodology. ; This research received essential financial support through the National Science and Technology Council (NSTC 112-2636-M-110-003 and Yushan Young Scholar Program of the Ministry of Education of Taiwan. The authors express their gratitude to Dr. Daniel Kaiser (University of Vienna) for proofreading our manuscript.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: unknown
تدمد: 1523-7060
1523-7052
Relation: Organic Letters; http://hdl.handle.net/10754/697635
DOI: 10.1021/acs.orglett.4c00677
الاتاحة: http://hdl.handle.net/10754/697635
https://doi.org/10.1021/acs.orglett.4c00677
Rights: Archived with thanks to Organic Letters under a Creative Commons license, details at: https://creativecommons.org/licenses/by/4.0/ ; https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.9119B8B5
قاعدة البيانات: BASE
الوصف
تدمد:15237060
15237052
DOI:10.1021/acs.orglett.4c00677