期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 43, 页码 11660-11664出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201403778
关键词
anion-binding catalysis; anion- interactions; organocatalysis; organofluorine compounds; pyridinium cations
资金
- SusChemSys
- Fonds der Chemischen Industrie
A new activation principle in organocatalysis is presented: halide binding through Coulombic interactions. This mode of catalysis was realized by using 3,5-di(carbomethoxy)pyridinium ions that carry an additional electron-withdrawing substituent on the nitrogen atom, for example, pentafluorobenzyl or cyanomethyl. For the N-pentafluorobenzyl derivative, Coulombic interaction with the pyridinium moiety is complemented in the solid state by anion- interactions with the perfluorophenyl ring. Bromide and chloride are bound by these cations in a 1:1 stoichiometry. Catalysis of the CC coupling between 1-chloroisochroman (and related electrophiles) with silyl ketene acetals occurs at -78 degrees C and at low catalyst loading (2 mol%).
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