Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315245 | Journal of Fluorine Chemistry | 2009 | 9 Pages |
Abstract
Treatment of (E)-4,4,4-trifluoro-1-aryl-2-buten-1-one with various aryldiazonium salts in the presence of palladium catalyst gave the corresponding α-arylated Heck adducts with high regio- and stereoselectivity in good to high yields.
Graphical abstractTreatment of (E)-4,4,4-trifluoro-1-aryl-2-buten-1-one with various aryldiazonium salts in the presence of palladium catalyst gave the corresponding α-arylated Heck adducts with high regio- and stereoselectivity in good to high yields.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Tsutomu Konno, Shigeyuki Yamada, Akinori Tani, Masataka Nishida, Tomotsugu Miyabe, Takashi Ishihara,