An Easy Route to (Hetero) arylboronic Acids
…, M Albini, J Rouden, J Blanchet
Index: Erb, William; Hellal, Akila; Albini, Mathieu; Rouden, Jacques; Blanchet, Jerome Chemistry - A European Journal, 2014 , vol. 20, # 22 p. 6608 - 6612
Full Text: HTML
Citation Number: 21
Abstract
Abstract An unprecedented spontaneous reactivity between diazonium salts and diboronic acid has been unveiled, leading to a versatile arylboronic acid synthesis directly from (hetero) arylamines. This fast reaction (35 min overall) tolerates a wide range of functional groups and is carried out under very mild conditions. The radical nature of the reaction mechanism has been investigated.
Related Articles:
[Zheng, Shi-Long; Reid, Suazette; Lin, Na; Wang, Binghe Tetrahedron Letters, 2006 , vol. 47, # 14 p. 2331 - 2335]
[Thoresen, Lars H.; Jiao, Guan-Sheng; Haaland, Wade C.; Metzker, Michael L.; Burgess, Kevin Chemistry - A European Journal, 2003 , vol. 9, # 19 p. 4603 - 4610]
[Wan, Chi-Wai; Burghart, Armin; Chen, Jiong; Bergstroem, Fredrik; Johansson, Lennart B.-A.; Wolford, Matthew F.; Kim, Taeg Gyum; Topp, Michael R.; Hochstrasser, Robin M.; Burgess, Kevin Chemistry - A European Journal, 2003 , vol. 9, # 18 p. 4430 - 4441]
[Zheng, Shi-Long; Reid, Suazette; Lin, Na; Wang, Binghe Tetrahedron Letters, 2006 , vol. 47, # 14 p. 2331 - 2335]