One-pot tandem synthesis of 2,3-unsubstituted indoles, an improved Leimgruber-Batchoindole synthesis
其他题名Phytoremediation of Cadmium-Contaminated Soil by Two Jerusalem Artichoke (Helianthus tuberosus L.) Genotypes.pdf
Chen, Jinchun1; Zhang, Zhikai1,2; Liu, Sujing2,3; Yang, Cuiyun2; Xia, Chuanhai2; Chen, JC (reprint author), Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China. [email protected]
发表期刊RSC ADVANCES
ISSN2046-2069
2014
卷号4期号:9页码:4672-4675
关键词Substituted Indoles Catalyzed Annulation 2 Convenient Synthesis 3-disubstituted Indoles Derivatives Functionalization Heterocycles Alkaloids Arylation Concise
产权排序[Chen, Jinchun; Zhang, Zhikai] Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China; [Zhang, Zhikai; Liu, Sujing; Yang, Cuiyun; Xia, Chuanhai] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resources Utilizat, Yantai 264003, Peoples R China; [Liu, Sujing] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
英文摘要A concise, fast and efficient one-pot methodology has been developed for preparing 2,3-unsubstituted indoles from 2-nitrotoluenes and dimethylformamide dimethyl acetal. Compared with the classical Leimgruber-Batcho reaction, such a one-pot process simplified the operation procedures, generated less by-products and chemical residues, and resulted in higher overall yields in a shorter reaction time.; A concise, fast and efficient one-pot methodology has been developed for preparing 2,3-unsubstituted indoles from 2-nitrotoluenes and dimethylformamide dimethyl acetal. Compared with the classical Leimgruber-Batcho reaction, such a one-pot process simplified the operation procedures, generated less by-products and chemical residues, and resulted in higher overall yields in a shorter reaction time.
文章类型Article
资助机构Yantai Science and Technology Development Project [2011063]; National Key Technology Research and Development Program [2011BAC02B04]; Cooperation Program of Chinese Academy of Sciences and District [Y12B051011]; K.C. Wong Education Foundation, Hongkong
收录类别SCI
语种英语
关键词[WOS]SUBSTITUTED INDOLES ; 2,3-DISUBSTITUTED INDOLES ; CATALYZED ANNULATION ; CONVENIENT SYNTHESIS ; DERIVATIVES ; FUNCTIONALIZATION ; HETEROCYCLES ; ALKALOIDS ; ARYLATION ; CONCISE
研究领域[WOS]Chemistry
WOS记录号WOS:000328956700056
引用统计
被引频次:9[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/7029
专题海岸带生物学与生物资源利用重点实验室_海岸带生物学与生物资源保护实验室
通讯作者Chen, JC (reprint author), Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China. [email protected]
作者单位1.Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China
2.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resources Utilizat, Yantai 264003, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
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GB/T 7714
Chen, Jinchun,Zhang, Zhikai,Liu, Sujing,et al. One-pot tandem synthesis of 2,3-unsubstituted indoles, an improved Leimgruber-Batchoindole synthesis[J]. RSC ADVANCES,2014,4(9):4672-4675.
APA Chen, Jinchun,Zhang, Zhikai,Liu, Sujing,Yang, Cuiyun,Xia, Chuanhai,&Chen, JC .(2014).One-pot tandem synthesis of 2,3-unsubstituted indoles, an improved Leimgruber-Batchoindole synthesis.RSC ADVANCES,4(9),4672-4675.
MLA Chen, Jinchun,et al."One-pot tandem synthesis of 2,3-unsubstituted indoles, an improved Leimgruber-Batchoindole synthesis".RSC ADVANCES 4.9(2014):4672-4675.
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