中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
One-pot tandem synthesis of 2,3-unsubstituted indoles, an improved Leimgruber-Batchoindole synthesis

文献类型:期刊论文

作者Chen, Jinchun1; Zhang, Zhikai1,2; Liu, Sujing2,3; Yang, Cuiyun2; Xia, Chuanhai2
刊名RSC ADVANCES
出版日期2014
卷号4期号:9页码:4672-4675
关键词SUBSTITUTED INDOLES 2 CATALYZED ANNULATION CONVENIENT SYNTHESIS DERIVATIVES FUNCTIONALIZATION HETEROCYCLES ALKALOIDS ARYLATION CONCISE 3-DISUBSTITUTED INDOLES
ISSN号2046-2069
其他题名Phytoremediation of Cadmium-Contaminated Soil by Two Jerusalem Artichoke (Helianthus tuberosus L.) Genotypes.pdf
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
通讯作者Chen, JC (reprint author), Yantai Univ, Coll Chem & Chem Engn, Yantai 264005, Peoples R China. chxia@yic.ac.cn
中文摘要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.
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.
学科主题Chemistry, Multidisciplinary
研究领域[WOS]Chemistry
关键词[WOS]SUBSTITUTED INDOLES ; 2,3-DISUBSTITUTED INDOLES ; CATALYZED ANNULATION ; CONVENIENT SYNTHESIS ; DERIVATIVES ; FUNCTIONALIZATION ; HETEROCYCLES ; ALKALOIDS ; ARYLATION ; CONCISE
收录类别SCI
资助信息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
原文出处http://dx.doi.org/10.1039/c3ra45548c
语种英语
WOS记录号WOS:000328956700056
公开日期2014-07-08
源URL[http://ir.yic.ac.cn/handle/133337/7029]  
专题烟台海岸带研究所_海岸带生物学与生物资源利用所重点实验室
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
推荐引用方式
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.(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.

入库方式: OAI收割

来源:烟台海岸带研究所

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