JOURNAL ARTICLE
Palladium-Catalyzed Suzuki−Miyaura Cross-Couplings of Aryl Tosylates with Potassium Aryltrifluoroborates
Year: 2007 Journal: The Journal of Organic Chemistry Vol: 72 (24)Pages: 9346-9349 Publisher: American Chemical Society
Abstract
Pd-catalyzed Suzuki-Miyaura cross-coupling reaction of aryl tosylates with potassium aryl trifluoroborate in the presence of bulky and electron-rich phosphine ligand is described. In addition, a useful chemoselective coupling of an aryl chloride in the presence of a tosyloxy group was demonstrated.
Keywords:
Chemistry Aryl Phosphine Palladium Catalysis Potassium Ligand (biochemistry) Coupling reaction Suzuki reaction Organic chemistry Chloride Medicinal chemistry Combinatorial chemistry Alkyl
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7
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0.98
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Citation History
Topics
Catalytic Cross-Coupling Reactions
Physical Sciences → Chemistry → Organic Chemistry
Chemical synthesis and alkaloids
Physical Sciences → Chemistry → Organic Chemistry
Organoboron and organosilicon chemistry
Physical Sciences → Chemistry → Organic Chemistry
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