中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Gold-Catalyzed Deacylative Cycloisomerization Reactions of 3-Acylindole/ynes: A New Approach for Carbazole Synthesis

文献类型:期刊论文

作者Wang L(王璐) ; Li GJ(李贵杰) ; Liu YH(刘元红)
刊名Org. Lett.
出版日期2011
卷号13期号:15页码:3786-3789
ISSN号1523-7060
其他题名金催化的3-酰基吲哚的环化去酰化反应: 咔唑化合物的新合成法研究
通讯作者刘元红
英文摘要The synthesis of functionalized carbazoles through gold-catalyzed deacylative cycloisomerization of 3-acylindole/ynes is described. A mechanistic proposal for these transformations involving a novel carbonyl group facilitated heterolytic fragmentation upon the loss of an acylium ion intermediate is presented. The eliminated acylium ion species could be trapped by the organogold intermediate to afford acylcarbazoles.
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/ol2012154
语种英语
WOS记录号WOS:000293252800005
公开日期2013-03-11
源URL[http://202.127.28.38/handle/331003/24307]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Wang L,Li GJ,Liu YH. Gold-Catalyzed Deacylative Cycloisomerization Reactions of 3-Acylindole/ynes: A New Approach for Carbazole Synthesis[J]. Org. Lett.,2011,13(15):3786-3789.
APA 王璐,李贵杰,&刘元红.(2011).Gold-Catalyzed Deacylative Cycloisomerization Reactions of 3-Acylindole/ynes: A New Approach for Carbazole Synthesis.Org. Lett.,13(15),3786-3789.
MLA 王璐,et al."Gold-Catalyzed Deacylative Cycloisomerization Reactions of 3-Acylindole/ynes: A New Approach for Carbazole Synthesis".Org. Lett. 13.15(2011):3786-3789.

入库方式: OAI收割

来源:上海有机化学研究所

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