ICCAS OpenIR
Efficient and Metal-Free Friedel-Crafts Alkylation of Indoles with Allyl Acetate Mediated by TFE
Liu, Zhe1,2; Liu, Li1; Wu, Yan-Chao1,2; Wang, Dong1
2010-12-01
Source PublicationLETTERS IN ORGANIC CHEMISTRY
ISSN1570-1786
Volume7Issue:8Pages:666-670
AbstractAn efficient, metal-free and chemo-selective Friedel-Crafts allylation of indoles in 2,2,2-trifluoroethanol (TFE) is developed. A possible mechanism has also been discussed to explain the observed competitive pathways in this reaction system.
KeywordIndole Friedel-crafts Alkylation 2 2 2-trifluoroethanol
Indexed BySCI
Language英语
WOS IDWOS:000287801700009
PublisherBENTHAM SCIENCE PUBL LTD
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Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/68696
Collection中国科学院化学研究所
Corresponding AuthorLiu, Li
Affiliation1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100080, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Liu, Zhe,Liu, Li,Wu, Yan-Chao,et al. Efficient and Metal-Free Friedel-Crafts Alkylation of Indoles with Allyl Acetate Mediated by TFE[J]. LETTERS IN ORGANIC CHEMISTRY,2010,7(8):666-670.
APA Liu, Zhe,Liu, Li,Wu, Yan-Chao,&Wang, Dong.(2010).Efficient and Metal-Free Friedel-Crafts Alkylation of Indoles with Allyl Acetate Mediated by TFE.LETTERS IN ORGANIC CHEMISTRY,7(8),666-670.
MLA Liu, Zhe,et al."Efficient and Metal-Free Friedel-Crafts Alkylation of Indoles with Allyl Acetate Mediated by TFE".LETTERS IN ORGANIC CHEMISTRY 7.8(2010):666-670.
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