A General Palladium??Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
CM So, CP Lau, FY Kwong
Index: So, Chau Ming; Lau, Chak Po; Kwong, Fuk Yee Angewandte Chemie - International Edition, 2008 , vol. 47, # 42 p. 8059 - 8063
Full Text: HTML
Citation Number: 133
Abstract
Palladium-catalyzed cross-coupling reactions have become an extremely versatile tool in organic synthesis for the connection of electrophilic and organometallic fragments by the formation of either carbon–carbon or carbon–heteroatom bonds.[1] In particular, the Suzuki– Miyaura reaction, employing organoboron nucleophiles, represents an effective method for the construction of C (sp2) ÀC (sp2) linkages, and has numerous applications in ...
Related Articles:
Palladium− Indolylphosphine-Catalyzed Hiyama Cross-Coupling of Aryl Mesylates
[So, Chau Ming; Lee, Hang Wai; Lau, Chak Po; Kwong, Fuk Yee Organic Letters, 2009 , vol. 11, # 2 p. 317 - 320]
[Quasdorf, Kyle W.; Antoft-Finch, Aurora; Liu, Peng; Silberstein, Amanda L.; Komaromi, Anna; Blackburn, Tom; Ramgren, Stephen D.; Houk; Snieckus, Victor; Garg, Neil K. Journal of the American Chemical Society, 2011 , vol. 133, # 16 p. 6352 - 6363]
Room-temperature photoinduced direct C–H-arylation via base-promoted homolytic aromatic substitution
[Buden, Maria E.; Guastavino, Javier F.; Rossi, Roberto A. Organic Letters, 2013 , vol. 15, # 6 p. 1174 - 1177]
[Journal of the American Chemical Society, , vol. 133, # 16 p. 6352 - 6363]