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One-pot construction of fused polycyclic heteroarenes involving 7-azaindoles and alpha,beta-unsaturated ketones
Li, Shuai-Shuai1,2,3; Li, Wei-Huan1; Zhang, Guo-Tai1; Xia, Ying-Qi1; Liu, Chen-Fei1; Su, Fu1; Zhang, Xiao-Mei2; Dong, Lin1
刊名Organic & biomolecular chemistry
2016
卷号14期号:33页码:7859-7863
ISSN号1477-0520
DOI10.1039/c6ob01437b
通讯作者Dong, lin(dongl@scu.edu.cn)
英文摘要A novel one-pot synthesis of pi-conjugated polycyclic compounds, which could undergo further facile transformation to form complex polycyclic heteroarene compounds, has been realized between 7-azaindoles and alpha,beta-unsaturated ketones. this distinctive cascade process proceeds via a rhodium(iii)-catalyzed alkylation/copper-catalyzed radical annulation-aromatization pathway.
WOS关键词C-H BONDS ; CONJUGATE ADDITION ; MILD CONDITIONS ; DERIVATIVES ; ACID ; ALKENYLATION ; CYCLIZATION ; ACTIVATION ; INHIBITORS ; ALKYLATION
WOS研究方向Chemistry
WOS类目Chemistry, Organic
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000382061100007
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/2375278
专题中国科学院大学
通讯作者Dong, Lin
作者单位1.Sichuan Univ, West China Sch Pharm, Educ Minist, Key Lab Drug Targeting & Drug Delivery Syst, Chengdu 610041, Peoples R China
2.Chinese Acad Sci, Chengdu Inst Organ Chem, Key Lab Asymmetr Synth & Chiral Technol Sichuan P, Chengdu 610041, Peoples R China
3.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Li, Shuai-Shuai,Li, Wei-Huan,Zhang, Guo-Tai,et al. One-pot construction of fused polycyclic heteroarenes involving 7-azaindoles and alpha,beta-unsaturated ketones[J]. Organic & biomolecular chemistry,2016,14(33):7859-7863.
APA Li, Shuai-Shuai.,Li, Wei-Huan.,Zhang, Guo-Tai.,Xia, Ying-Qi.,Liu, Chen-Fei.,...&Dong, Lin.(2016).One-pot construction of fused polycyclic heteroarenes involving 7-azaindoles and alpha,beta-unsaturated ketones.Organic & biomolecular chemistry,14(33),7859-7863.
MLA Li, Shuai-Shuai,et al."One-pot construction of fused polycyclic heteroarenes involving 7-azaindoles and alpha,beta-unsaturated ketones".Organic & biomolecular chemistry 14.33(2016):7859-7863.
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