Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315706 | Journal of Fluorine Chemistry | 2006 | 7 Pages |
Abstract
Treatment of fluoroalkylated alkynes with various aryl halides and arylboronic acids in the presence of Pd(0) in DMF/H2O at 100 °C for 2 h led to the smooth three-component coupling reaction, the corresponding tetrasubstituted alkenes being obtained in high yields stereoselectively.
Graphical abstractFluorine-containing tetrasubstituted alkenes were synthesized in an one-pot via palladium-catalyzed three-component coupling reaction using fluoroalkylated alkyens, aryl iodides and arylboronic acids. Figure optionsDownload full-size imageDownload as PowerPoint slide
Keywords
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Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Tsutomu Konno, Ken-ichi Taku, Takashi Ishihara,