Acid-Promoted Cross-Dehydrative Aromatization for the Synthesis of Tetraaryl-Substituted Pyrroles
文献类型:期刊论文
作者 | Wu, Xudong1; Li, Ke1; Wang, Siyuan1; Liu C(刘超)1,2; Lei AW(雷爱文)1 |
刊名 | Organic Letters
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出版日期 | 2016 |
卷号 | 18期号:1页码:56-59 |
ISSN号 | 1523-7060 |
通讯作者 | 刘超 ; 雷爱文 |
英文摘要 | Tetraaryl-substituted pyrroles are one important class of luminophores. In this work, an acid-promoted cross-dehydrative aromatization between benzoin and deoxybenzion was developed. This transformation provides an efficient and straightforward path for the synthesis of various aryl group substituted tetraarylpyrroles. Good to excellent yields were obtained through the easy operation with acetic acid and ammonium acetate. |
学科主题 | 物理化学与绿色催化 |
收录类别 | SCI |
资助信息 | the 973 Program (2012CB725302);the National Natural Science Foundation of China (21390400;21520102003;21272180;21302148);the Hubei Province Natural Science Foundation of China (2013CFA081);the Research Fund for the Doctoral Program of Higher Education of China (20120141130002);the Ministry of Science and Technology of China (2012YQ120060);The Program of Introducing Talents of Discipline to Universities of China (111 Program) |
语种 | 英语 |
WOS记录号 | WOS:000367702400015 |
源URL | [http://210.77.64.217/handle/362003/19393] ![]() |
专题 | 兰州化学物理研究所_OSSO国家重点实验室 |
作者单位 | 1.Wuhan Univ, IAS, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China 2.Chinese Acad Sci, LICP, Suzhou Res Inst, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China |
推荐引用方式 GB/T 7714 | Wu, Xudong,Li, Ke,Wang, Siyuan,et al. Acid-Promoted Cross-Dehydrative Aromatization for the Synthesis of Tetraaryl-Substituted Pyrroles[J]. Organic Letters,2016,18(1):56-59. |
APA | Wu, Xudong,Li, Ke,Wang, Siyuan,Liu C,&Lei AW.(2016).Acid-Promoted Cross-Dehydrative Aromatization for the Synthesis of Tetraaryl-Substituted Pyrroles.Organic Letters,18(1),56-59. |
MLA | Wu, Xudong,et al."Acid-Promoted Cross-Dehydrative Aromatization for the Synthesis of Tetraaryl-Substituted Pyrroles".Organic Letters 18.1(2016):56-59. |
入库方式: OAI收割
来源:兰州化学物理研究所
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