Efficient Carbazole Synthesis via Pd/Cu-Cocatalyzed Cross-Coupling/Isomerization of 2-Allyl-3-iodoindoles and Terminal Alkynes
Zhu C(朱灿)1; Ma SM(麻生明)1
刊名Org. Lett.
2014
卷号16期号:6页码:1542-1545
其他题名通过钯/铜共催化的2-烯丙基-3-碘代吲哚和末端炔烃的交叉偶联/异构化反应有效合成咔唑的方法
通讯作者麻生明
英文摘要The Pd/Cu-cocatalyzed one-pot reaction of 2-allyl-3-iodo-1-tosyl-1H-indoles and terminal alkynes afforded carbazoles highly efficiently via sequential carbon carbon coupling, isomerization, cyclization, and aromatization forming a benzene ring. Both Pd and Cu are responsible for the coupling step, while K2CO3 was observed to be critical for the subsequent cyclization.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ol500119r
语种英语
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39047]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位1.中科院上海有机化学研究所
2.华东师范大学
推荐引用方式
GB/T 7714
Zhu C,Ma SM. Efficient Carbazole Synthesis via Pd/Cu-Cocatalyzed Cross-Coupling/Isomerization of 2-Allyl-3-iodoindoles and Terminal Alkynes[J]. Org. Lett.,2014,16(6):1542-1545.
APA 朱灿,&麻生明.(2014).Efficient Carbazole Synthesis via Pd/Cu-Cocatalyzed Cross-Coupling/Isomerization of 2-Allyl-3-iodoindoles and Terminal Alkynes.Org. Lett.,16(6),1542-1545.
MLA 朱灿,et al."Efficient Carbazole Synthesis via Pd/Cu-Cocatalyzed Cross-Coupling/Isomerization of 2-Allyl-3-iodoindoles and Terminal Alkynes".Org. Lett. 16.6(2014):1542-1545.
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