Efficient pyridylbenzamidine ligands for palladium-catalyzed Suzuki-Miyaura reaction
✍ Scribed by Huang, Ying-Tang; Tang, Xiao; Yang, Yi; Shen, Dong-Sheng; Tan, Cheng; Liu, Feng-Shou
- Book ID
- 118752506
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 234 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0268-2605
- DOI
- 10.1002/aoc.2913
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📜 SIMILAR VOLUMES
A simple catalytic system based on PdCl 2 and triphenylphosphine chalcogenides (PPh 3 X; X = O, S, Se) is found to be highly effective (up to 97% isolated yield) in the room temperature Suzuki-Miyaura reactions. Under the same experimental conditions, triphenylphosphine chalcogenides as ligands show
Suzuki-Miyaura cross-coupling reaction has been achieved under the catalysis of Pd(OAc) 2 in the presence of readily accessible and easily tunable aminophosphine ligands with high efficiency under mild reaction condition.
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