A rapid, solvent-free, ligandless and mild method for preparing aromatic ketones from acyl chlorides and arylboronic acids via a Suzuki–Miyaura type of coupling reaction

2005 ◽  
Vol 46 (44) ◽  
pp. 7627-7630 ◽  
Author(s):  
B.P. Bandgar ◽  
A.V. Patil
Keyword(s):  
Coupling Reaction ◽  
Solvent Free ◽  
Aromatic Ketones ◽  
Acyl Chlorides ◽  
Arylboronic Acids

Eco-friendly Suzuki–Miyaura coupling of arylboronic acids to aromatic ketones catalyzed by the oxime-palladacycle in biosolvent 2-MeTHF

2016 ◽  
Vol 40 (4) ◽  
pp. 3119-3123 ◽  
Author(s):  
Manoj Mondal ◽  
Utpal Bora
Keyword(s):  
Green Chemistry ◽  
Sugar Cane ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Aromatic Ketones ◽  
Acyl Chlorides ◽  
Arylboronic Acids ◽  
Cross Coupling Reaction ◽  
Reaction Proceeds ◽  
Aryl Ketones

Oxime-palladacycle catalyzed aerobic cross-coupling reaction of arylboronic acids and acyl chlorides to yield aryl ketones was developed. The reaction proceeds efficiently in 2-MeTHF, which is derived from corncobs, sugar cane, and fulfils the 3rd, 5th and 7th principles of Green Chemistry.

Sign in / Sign up

Export Citation Format

Share Document