抄録
The palladium-catalyzed cross-coupling reactions of acid chlorides with arylboronic acids in the presence of copper(I) thiophene-2-carboxylate (CuTC) as an activator under strictly non-basic and mild reaction conditions afford the unsymmetrical ketones in moderate to excellent yields. A wide range of substrates bearing an electron-donating or an electron-withdrawing substituent on the aromatic ring is compatible.
本文言語 | English |
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ページ(範囲) | 2309-2312 |
ページ数 | 4 |
ジャーナル | Synlett |
号 | 15 |
DOI | |
出版ステータス | Published - 9月 19 2005 |
ASJC Scopus subject areas
- 有機化学