Palladium-Catalyzed Suzuki-Miyaura Type Coupling Reaction of Aryl Halides with Triphenylborane-Pyridine
The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd（OAc）2 （5 mol%） in presence of Cs2CO3 at 50 ℃ or 80 ℃, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tole...
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| Published in | Chinese journal of chemistry Vol. 30; no. 10; pp. 2581 - 2586 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
01.10.2012
WILEY‐VCH Verlag Wiley Wiley Subscription Services, Inc |
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| Online Access | Get full text |
| ISSN | 1001-604X 1614-7065 |
| DOI | 10.1002/cjoc.201200775 |
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| Abstract | The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd（OAc）2 （5 mol%） in presence of Cs2CO3 at 50 ℃ or 80 ℃, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of func- tional groups. |
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| AbstractList | The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in presence of Cs2CO3 at 50°C or 80°C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. [PUBLICATION ABSTRACT] The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd（OAc）2 （5 mol%） in presence of Cs2CO3 at 50 ℃ or 80 ℃, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of func- tional groups. The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc) 2 (5 mol%) in presence of Cs 2 CO 3 at 50°C or 80°C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in presence of Cs2CO3 at 50 degrees C or 80 degrees C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in presence of Cs2CO3 at 50°C or 80°C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in the presence of Cs2CO3 at 50°C or 80°C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. |
| Author | Yang, Minghua Yan, Guobing Gu, Yongbing Zhao, Xiyu Wang, Yan |
| AuthorAffiliation | Department of Chemistry, Lishui University, Lishui, Zhejiang 323000, China |
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| Copyright | Copyright © 2012 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2012 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
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| Keywords | BORONIC ACIDS aryl halides palladium catalysts triphenylbroane-pyridine COMPLEXES ARENES CONVENIENT Suzuki-Miyaura coupling COMBINATION |
| Language | English |
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| Notes | 31-1547/O6 The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd（OAc）2 （5 mol%） in presence of Cs2CO3 at 50 ℃ or 80 ℃, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of func- tional groups. Yang, Minghua Gu, Yongbing Wang, Yan Zhao, Xiyu Yan, Guobing Department of Chemistry, Lishui University, Lishui, Zhejiang 323000, China triphenylbroane-pyridine, Suzuki-Miyaura coupling, aryl halides, palladium catalysts istex:467EEFB57C984B12C609A769E38EF6D9F670E2BF the Research Foundation of Education Department of Zhejiang Province - No. YZ01018492 ark:/67375/WNG-8GP7TTXS-D ArticleID:CJOC201200775 the Natural Science Foundation of Zhejiang Province - No. Y407081 ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 |
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| Snippet | The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd（OAc）2 （5 mol%） in... The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in... The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc) 2 (5 mol%) in... The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in... |
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| SubjectTerms | aryl halides Chemistry Chemistry, Multidisciplinary Halides Palladium palladium catalysts Physical Sciences Science & Technology Suzuki-Miyaura coupling triphenylbroane-pyridine 三苯基 偶联反应 催化反应 吡啶 碳酸铯 类型 芳基卤化物 钯催化 |
| Title | Palladium-Catalyzed Suzuki-Miyaura Type Coupling Reaction of Aryl Halides with Triphenylborane-Pyridine |
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