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FluoroFusion: NHC-Catalyzed Nucleophilic Aromatic Substitution Reaction Unveils Functional Perfluorinated Diarylmethanones.
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.
Afiliação
  • Chan CL; Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Lee SC; Department of International Ph.D. Program for Science, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Lin PS; Department of Chemistry, National Chung Hsing University, Taichung 402202, Taiwan (R.O.C.).
  • Tapales RVPP; KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955, Saudi Arabia.
  • Li JS; Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Lai CA; Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Lee JT; Department of International Ph.D. Program for Science, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Li CH; Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
  • Liao HH; Department of Chemistry, National Sun Yat-sen University, Kaohsiung 804201, Taiwan (R.O.C.).
Org Lett ; 26(11): 2338-2342, 2024 Mar 22.
Article em En | MEDLINE | ID: mdl-38458971
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article