Alkoxycarbonylation reactions using aryl fluorosulfonates
GP Roth, JA Thomas
Index: Roth, Gregory P.; Thomas, Jeanine A. Tetrahedron Letters, 1992 , vol. 33, # 15 p. 1959 - 1962
Full Text: HTML
Citation Number: 18
Abstract
There are several accounts in the literature describing the transition metal catalyzed carbonylation of aryl halides and aryl triflates in the presence of an alcohol or amine to provide the corresponding ester or amide product. This direct introduction of a carbonyl group into a molecule can be accomplished by a variety of methods. Cacchi, Ortar, and coworkers1 have reported that a variety of enol and aryl triflates readily undergo oxidative addition to palladium followed by migratory ...
Related Articles:
[Salvadori, Jessica; Balducci, Evita; Zaza, Silvia; Petricci, Elena; Taddei, Maurizio Journal of Organic Chemistry, 2010 , vol. 75, # 6 p. 1841 - 1847]
[Yamakawa, Takeshi; Kinoshita, Hidenori; Miura, Katsukiyo Journal of Organometallic Chemistry, 2013 , vol. 724, p. 129 - 134]
[Yamakawa, Takeshi; Kinoshita, Hidenori; Miura, Katsukiyo Journal of Organometallic Chemistry, 2013 , vol. 724, p. 129 - 134]
[Ben-David, Yehoshua; Portnoy, Moshe; Milstein, David Journal of the American Chemical Society, 1989 , vol. 111, # 23 p. 8742 - 8744]
[Ram, Ram N.; Soni, Vineet Kumar; Gupta, Dharmendra Kumar Tetrahedron, 2012 , vol. 68, # 44 p. 9068 - 9075]