Novel catalytic CO2 incorporation reaction:: Nickel-catalyzed regio- and stereoselective ring-closing carboxylation of bis-1,3-dienes

被引:157
作者
Takimoto, M [1 ]
Mori, M [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
关键词
D O I
10.1021/ja026620c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel nickel-catalyzed carboxylation of bis-1,3-dienes using carbon dioxide (CO2) was investigated. In the presence of catalytic amounts of Ni(acac)2 and PPh3, various bis-1,3-dienes smoothly reacted with CO2 and an organozinc reagent (Et2Zn, Me2Zn, or Ph2Zn) under mild conditions. This catalytic carboxylation process was accompanied by carbocyclization of bis-1,3-diene followed by alkylation by an organozinc reagent to afford cyclic carboxylic acid derivatives in high yields with high regio- and stereoselectivities. Copyright © 2002 American Chemical Society.
引用
收藏
页码:10008 / 10009
页数:2
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