Palladium-catalyzed Coupling between Aryl Halides and Trimethylsilylacetylene Assisted by Dimethylaminotrimethyltin
Palladium-catalyzed coupling between aryl halides, especially less reactive ones or N-heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents.
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| Published in | Chinese journal of chemistry Vol. 29; no. 5; pp. 1059 - 1062 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
01.05.2011
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1001-604X 1614-7065 |
| DOI | 10.1002/cjoc.201190180 |
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| Abstract | Palladium-catalyzed coupling between aryl halides, especially less reactive ones or N-heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents. |
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| AbstractList | Palladium‐catalyzed coupling between aryl halides, especially less reactive ones or N‐heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents.
Palladium‐catalyzed coupling between aryl halides, especially less reactive ones or N‐heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents. Palladium-catalyzed coupling between aryl halides, especially less reactive ones or N-heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents. Palladium‐catalyzed coupling between aryl halides, especially less reactive ones or N ‐heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents. |
| Author | Cai, Liangzhen Tao, Xiaochun Sun, Zhonghua Cai, Lisheng Pike, Victor W. Yang, Dujuan |
| AuthorAffiliation | School of Chemical and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, U. S. A. |
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| Cites_doi | 10.1016/j.tetlet.2008.09.060 10.1021/ja00241a035 10.1002/anie.198605081 10.1016/S0040-4039(00)91094-3 10.1021/jm0702231 10.1021/cr050992x 10.1021/jm950934b 10.1016/j.bmcl.2008.05.071 10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U 10.1016/S0022-328X(02)01158-0 10.1080/00304949509458449 10.1002/anie.200602761 10.1021/jo9808021 10.1016/j.jorganchem.2003.07.028 10.1016/S0960-894X(99)00277-2 10.1021/jm700970s 10.1021/jo701458b 10.1016/j.cclet.2008.05.016 10.1002/adsc.200606033 10.1021/jm990134r 10.1002/9783527612222.ch5 10.1021/om0303754 10.1039/a607060d 10.1021/ol0257732 10.1021/ja064479s |
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| Copyright | Copyright © 2011 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2011 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
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| Keywords | Sonogashira coupling VINYL palladium catalysis COMPLEX SONOGASHIRA REAGENTS BETA-AMYLOID PLAQUES trimethylsilylacetylene dimethylaminotrimethyltin TERMINAL ALKYNES aryl halide |
| Language | English |
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| Notes | 31-1547/O6 palladium catalysis, trimethylsilylacetylene, aryl halide, dimethylaminotrimethyltin, Sonogashira coupling Cai Liangzhen, Yang Dujuan, Sun Zhonghua, Tao Xiaochun,Cai Lisheng,Pike Victor W.（a School of Chemical and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China b Molecular Imaging Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, U. S. A.） Palladium-catalyzed coupling between aryl halides, especially less reactive ones or N-heteroaryls, and trimethylsilylacetylene in the presence of dimethylaminotrimethyltin generated the coupled products in high yields. The reaction does not need CuI and base as auxiliary agents. ArticleID:CJOC201190180 istex:B0AE74C15FF943DACCBC3095C43EAB7A5D95EFDE ark:/67375/WNG-302H5ZQ9-N ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
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| SubjectTerms | aryl halide Chemistry Chemistry, Multidisciplinary dimethylaminotrimethyltin Halides Palladium palladium catalysis Physical Sciences Science & Technology Sonogashira coupling trimethylsilylacetylene 产量高 卤代芳烃 耦合 钯催化 |
| Title | Palladium-catalyzed Coupling between Aryl Halides and Trimethylsilylacetylene Assisted by Dimethylaminotrimethyltin |
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