Enantioselective N-Heterocyclic Carbene-Catalyzed Synthesis of Spirocyclic Oxindole-benzofuroazepinones | |
Gao, Zhong-Hua1; Chen, Kun-Quan1; Zhang, Yan1; Kong, Ling-Mei2; Li, Yan2,3; Ye, Song1,3 | |
2018-12-21 | |
发表期刊 | JOURNAL OF ORGANIC CHEMISTRY |
ISSN | 0022-3263 |
卷号 | 83期号:24页码:15225-15235 |
摘要 | Herein, we report an enantioselective synthesis of azepinones via the N-heterocyclic carbene (NHC) catalyzed [3+4] annulation reaction of isatin-derived enals and aurone-derived azadienes. The corresponding spirocyclic oxindole-benzofuroazepinones were obtained in good yields, with excellent diastereo- and enantioselectivities. The resulted azepinones were evaluated for their in vitro cytotoxic activities against six human tumor cell lines, with two compounds showing significant inhibitory activity comparable with that of cisplatin. |
收录类别 | SCI |
语种 | 英语 |
文献类型 | 期刊论文 |
条目标识符 | http://ir.kib.ac.cn/handle/151853/64351 |
专题 | 植物化学与西部植物资源持续利用国家重点实验室 |
通讯作者 | Li, Yan; Ye, Song |
作者单位 | 1.Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China 2.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China 3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Gao, Zhong-Hua,Chen, Kun-Quan,Zhang, Yan,et al. Enantioselective N-Heterocyclic Carbene-Catalyzed Synthesis of Spirocyclic Oxindole-benzofuroazepinones[J]. JOURNAL OF ORGANIC CHEMISTRY,2018,83(24):15225-15235. |
APA | Gao, Zhong-Hua,Chen, Kun-Quan,Zhang, Yan,Kong, Ling-Mei,Li, Yan,&Ye, Song.(2018).Enantioselective N-Heterocyclic Carbene-Catalyzed Synthesis of Spirocyclic Oxindole-benzofuroazepinones.JOURNAL OF ORGANIC CHEMISTRY,83(24),15225-15235. |
MLA | Gao, Zhong-Hua,et al."Enantioselective N-Heterocyclic Carbene-Catalyzed Synthesis of Spirocyclic Oxindole-benzofuroazepinones".JOURNAL OF ORGANIC CHEMISTRY 83.24(2018):15225-15235. |
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