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钌催化的N-芳基吡唑的C-H/CO/烯烃偶联反应。N-芳基吡唑对C-H键羰基化的非凡反应活性。

Ruthenium-catalyzed C-H/CO/Olefin coupling reaction of N-arylpyrazoles. Extraordinary reactivity of N-arylpyrazoles toward carbonylation at C-H bonds.

作者信息

Asaumi Taku, Chatani Naoto, Matsuo Takuya, Kakiuchi Fumitoshi, Murai Shinji

机构信息

Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

J Org Chem. 2003 Sep 19;68(19):7538-40. doi: 10.1021/jo0343127.

Abstract

The reaction of 1-arylpyrazoles with CO and ethylene in the presence of Ru(3)(CO)(12) resulted in regioselective carbonylation at the ortho C-H bonds. While it is found that the pyrazole ring also functions as the directing group for C-H bond cleavage, the efficiency of the reaction depends on the position of the pyrazole ring.

摘要

在Ru(3)(CO)(12)存在下,1-芳基吡唑与CO和乙烯反应,导致在邻位C-H键处发生区域选择性羰基化。虽然发现吡唑环也作为C-H键裂解的导向基团,但反应效率取决于吡唑环的位置。

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