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![]() ![]() |
刊名 | MOLECULAR DIVERSITY
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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 |
DOI | 10.1007/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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