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L-Proline promoted Ullmann-type coupling reactions of aryl iodides with indoles, pyrroles, imidazoles or pyrazoles
Alternative TitleL-Proline promoted Ullmann-type coupling reactions of aryl iodides with indoles, pyrroles, imidazoles or pyrazoles
Ma DW(马大为); Cai Q(蔡倩)
2004
Source PublicationSynlett
ISSN0936-5214
Issue1Pages:128-130
AbstractThe Ullmann-type coupling reactions of aryl iodides and several nitrogen heterocycles occur at 80-90 degreesC with L-proline as additive, giving N-arylpyrroles, N-arylindoles, N-arylimidazoles, and N-pyrazoles in good to excellent yields.
Subject Area生命有机化学
Department中国科学院上海有机化学研究所生命有机化学实验室
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Indexed BySCI
Language英语
WOS IDWOS:000187995800028
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/15471
Collection生命有机化学国家重点实验室
Corresponding AuthorMa DW(马大为)
Recommended Citation
GB/T 7714
Ma DW,Cai Q. L-Proline promoted Ullmann-type coupling reactions of aryl iodides with indoles, pyrroles, imidazoles or pyrazoles[J]. Synlett,2004(1):128-130.
APA 马大为,&蔡倩.(2004).L-Proline promoted Ullmann-type coupling reactions of aryl iodides with indoles, pyrroles, imidazoles or pyrazoles.Synlett(1),128-130.
MLA 马大为,et al."L-Proline promoted Ullmann-type coupling reactions of aryl iodides with indoles, pyrroles, imidazoles or pyrazoles".Synlett .1(2004):128-130.
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