中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Facile synthesis of indole- or benzofuran-fused benzo[a]carbazole-1,4-diones using a tandem two-step reaction sequence

文献类型:期刊论文

作者Tu, Shanghui1,2; Ding, Chunyong1,3; Hu, Wenxiang2; Li, Fulong1,3; Yao, Qizheng3; Zhang, Ao1
刊名MOLECULAR DIVERSITY
出版日期2011-02
卷号15期号:1页码:91-99
关键词Carbazole Anticancer Tandem reaction Coupling reaction Cyclization
ISSN号1381-1991
DOI10.1007/s11030-010-9241-x
文献子类Article
英文摘要An efficient three-step approach was developed to assemble indole- or benzofuran-fused benzocarbazole-1,4-diones in 42-53% overall yield. This approach includes AgOAc-promoted oxidative cyclization of 2,6-di-bromocyclohexene-1,4-dione with indol-3-ylpropanoid acid, condensation of the resulting bromocarbazole intermediates with phenols or anilines, followed by Pd(OAc)-catalyzed cyclization. Such convenient synthetic protocol and the novelty of the corresponding products will largely assist our drug design and development program.
WOS关键词VITRO ANTIPROLIFERATIVE ACTIVITIES ; CHECKPOINT-1 KINASE INHIBITORS ; BIOLOGICAL-ACTIVITIES ; GRANULATIMIDE ANALOGS ; COUPLING REACTIONS ; REBECCAMYCIN ; ANTITUMOR ; CARBAZOLES ; BEARING ; DERIVATIVES
资助项目Chinese National Science Foundation[30772625] ; National Science and Technology Major Project on "Key New Drug Creation and Manufacturing Program"[2009ZX09301-001] ; National Science and Technology Major Project on "Key New Drug Creation and Manufacturing Program"[2009ZX09103-062] ; "863" grant[2007AA022163] ; Chinese Academy of Sciences[00000000]
WOS研究方向Biochemistry & Molecular Biology ; Chemistry ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000288460200007
出版者SPRINGER
源URL[http://119.78.100.183/handle/2S10ELR8/278608]  
专题药物化学研究室
通讯作者Zhang, Ao
作者单位1.SIMM, SOMCL, Shanghai 201203, Peoples R China;
2.Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China;
3.China Pharmaceut Univ, Dept Med Chem, Nanjing 21009, Peoples R China
推荐引用方式
GB/T 7714
Tu, Shanghui,Ding, Chunyong,Hu, Wenxiang,et al. Facile synthesis of indole- or benzofuran-fused benzo[a]carbazole-1,4-diones using a tandem two-step reaction sequence[J]. MOLECULAR DIVERSITY,2011,15(1):91-99.
APA Tu, Shanghui,Ding, Chunyong,Hu, Wenxiang,Li, Fulong,Yao, Qizheng,&Zhang, Ao.(2011).Facile synthesis of indole- or benzofuran-fused benzo[a]carbazole-1,4-diones using a tandem two-step reaction sequence.MOLECULAR DIVERSITY,15(1),91-99.
MLA Tu, Shanghui,et al."Facile synthesis of indole- or benzofuran-fused benzo[a]carbazole-1,4-diones using a tandem two-step reaction sequence".MOLECULAR DIVERSITY 15.1(2011):91-99.

入库方式: OAI收割

来源:上海药物研究所

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