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 |
Subjects | |
Online Access | Get full text |
ISSN | 1001-604X 1614-7065 |
DOI | 10.1002/cjoc.201200775 |
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Summary: | 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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Bibliography: | 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 |
ISSN: | 1001-604X 1614-7065 |
DOI: | 10.1002/cjoc.201200775 |