Palladium-catalyzed ligand-free and aqueous Suzuki reaction for the construction of (hetero)aryl-substituted triphenylamine derivatives
出版年份 2012 全文链接
标题
Palladium-catalyzed ligand-free and aqueous Suzuki reaction for the construction of (hetero)aryl-substituted triphenylamine derivatives
作者
关键词
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出版物
RSC Advances
Volume 3, Issue 2, Pages 526-531
出版商
Royal Society of Chemistry (RSC)
发表日期
2012-11-07
DOI
10.1039/c2ra22275b
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- Oxygen-promoted PdCl2-catalyzed ligand-free Suzuki reaction in aqueous media
- (2010) Chun Liu et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- A fast and oxygen-promoted protocol for the ligand-free Suzuki reaction of 2-halogenated pyridines in aqueous media
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- (2009) Chris S. K. Mak et al. CHEMISTRY OF MATERIALS
- Manipulating Charge-Transfer Character with Electron-Withdrawing Main-Group Moieties for the Color Tuning of Iridium Electrophosphors
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