中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
[4+2] Cycloaddition of in Situ Generated 1,2-Diaza-1,3-dienes with Simple Olefins: Facile Approaches to Tetrahydropyridazines

文献类型:期刊论文

作者Zhong, Xingren1,2; Lv, Jian1,2; Luo, Sanzhong1,2
刊名ORGANIC LETTERS
出版日期2015-03-20
卷号17期号:6页码:1561-1564
英文摘要A catalyst-free [4 + 2] annulation process between in situ generated 1,2-diaza-1,3-butadienes and simple olefins has been developed. Under mild conditions, the reactions afforded 1,4,5,6-tetrahydropyridazines, which feature a wide range of bioactive compounds, with high yields (up to 99% yield).
收录类别SCI
语种英语
公开日期2015-11-03
源URL[http://ir.iccas.ac.cn/handle/121111/28466]  
专题化学研究所_分子识别与功能实验室
作者单位1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, BNLMS, Beijing 100190, Peoples R China
2.Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
推荐引用方式
GB/T 7714
Zhong, Xingren,Lv, Jian,Luo, Sanzhong. [4+2] Cycloaddition of in Situ Generated 1,2-Diaza-1,3-dienes with Simple Olefins: Facile Approaches to Tetrahydropyridazines[J]. ORGANIC LETTERS,2015,17(6):1561-1564.
APA Zhong, Xingren,Lv, Jian,&Luo, Sanzhong.(2015).[4+2] Cycloaddition of in Situ Generated 1,2-Diaza-1,3-dienes with Simple Olefins: Facile Approaches to Tetrahydropyridazines.ORGANIC LETTERS,17(6),1561-1564.
MLA Zhong, Xingren,et al."[4+2] Cycloaddition of in Situ Generated 1,2-Diaza-1,3-dienes with Simple Olefins: Facile Approaches to Tetrahydropyridazines".ORGANIC LETTERS 17.6(2015):1561-1564.

入库方式: OAI收割

来源:化学研究所

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