Imidate as the Intact Directing Group for the Cobalt-Catalyzed C-H Allylation

被引:25
|
作者
Tanaka, Ryo [1 ]
Tanimoto, Iku [1 ]
Kojima, Masahiro [1 ]
Yoshino, Tatsuhiko [1 ]
Matsunaga, Shigeki [1 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
来源
JOURNAL OF ORGANIC CHEMISTRY | 2019年 / 84卷 / 20期
关键词
ACTIVATION; FUNCTIONALIZATION; ISOQUINOLINES; ACCESS; COUPLING/CYCLIZATION; 1H-INDAZOLES; QUINAZOLINES; CYCLIZATION; AMIDATION; OLEFINS;
D O I
10.1021/acs.joc.9b01972
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cobalt-catalyzed C-H allylation reactions of NH-free benzimidate using vinylcyclopropanes or allyl carbonate are reported. The reactive and relatively unstable imidate groups remain intact during the C-H allylations to afford functionalized imidates without dealcoholizations. The thus obtained allylated imidate was subsequently converted into other heterocyclic structures through a following C-H functionalization reaction, demonstrating the synthetic utility of this method.
引用
收藏
页码:13203 / 13210
页数:8
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