Highly Efficient Suzuki-Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost-Effective [1,3-Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading
出版年份 2011 全文链接
标题
Highly Efficient Suzuki-Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost-Effective [1,3-Bis(diphenylphosphino)propane]nickel(II) Chloride [Ni(dppp)Cl2] with only 1 mol% Loading
作者
关键词
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出版物
ADVANCED SYNTHESIS & CATALYSIS
Volume 353, Issue 2-3, Pages 309-314
出版商
Wiley
发表日期
2011-01-19
DOI
10.1002/adsc.201000710
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- (2010) Jeanne L. Bolliger et al. CHEMISTRY-A EUROPEAN JOURNAL
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- (2009) François-Xavier Felpin et al. ADVANCED SYNTHESIS & CATALYSIS
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- (2009) Lukas J. Gooßen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- (2009) Brijesh Bhayana et al. ORGANIC LETTERS
- A General Palladium-Catalyzed Suzuki-Miyaura Coupling of Aryl Mesylates
- (2008) Chau Ming So et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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- Metallosupramolecular Polyelectrolytes Self-Assembled from Various Pyridine Ring-Substituted Bisterpyridines and Metal Ions: Photophysical, Electrochemical, and Electrochromic Properties
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- (2008) Fu-She Han et al. TETRAHEDRON
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