Copper‐Catalyzed Oxidative Cross‐Coupling of Electron‐Deficient Polyfluorophenylboronate Esters with Terminal Alkynes
Autor: | Alexandra Friedrich, Todd B. Marder, Mingming Huang, Udo Radius, Zhiqiang Liu, Stephen A. Westcott, Ya-Ming Tian, Yudha P. Budiman |
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Rok vydání: | 2020 |
Předmět: |
fluoroarenes
chemistry.chemical_element Sonogashira coupling Oxidative phosphorylation coupling reactions 010402 general chemistry 01 natural sciences Catalysis Coupling reaction chemistry.chemical_compound Full Paper 010405 organic chemistry Organic Chemistry Substrate (chemistry) Fluorine General Chemistry Full Papers Combinatorial chemistry 0104 chemical sciences Coupling (electronics) chemistry Terminal (electronics) ddc:540 Functional group Sonogashira reaction boronate esters |
Zdroj: | Chemistry (Weinheim an Der Bergstrasse, Germany) |
ISSN: | 1521-3765 0947-6539 |
Popis: | We report herein a mild procedure for the copper‐catalyzed oxidative cross‐coupling of electron‐deficient polyfluorophenylboronate esters with terminal alkynes. This method displays good functional group tolerance and broad substrate scope, generating cross‐coupled alkynyl(fluoro)arene products in moderate to excellent yields. Thus, it represents a simple alternative to the conventional Sonogashira reaction. BFF: A mild procedure is reported for the synthesis of alkynyl(fluoro)arenes via copper‐catalyzed oxidative cross‐coupling of polyfluorophenylboronate esters with terminal alkynes. |
Databáze: | OpenAIRE |
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