Potassium Alkenyl-and Aryltrifluoroborates: Stable and Efficient Agents for Rhodium-Catalyzed Addition to Aldehydes and Enones
RA Batey, AN Thadani, DV Smil
Index: Batey, Robert A.; Thadani, Avinash N.; Smil, David V. Organic Letters, 1999 , vol. 1, # 10 p. 1683 - 1686
Full Text: HTML
Citation Number: 195
Abstract
Potassium alkenyl-and aryltrifluoroborates undergo addition to enones and aldehydes in the presence of Rh (I) catalysts to give β-functionalized ketones and allylic/benzylic alcohols, respectively. Reaction proceeds more rapidly than with the corresponding boronic acids, and the choice of phosphine ligand does not signifcantly influence the overall efficiency of addition.
Related Articles:
Nickel??Catalyzed Electrochemical Arylation of Activated Olefins
[Condon, Sylvie; Dupre, Daniel; Falgayrac, Gilles; Nedelec, Jean-Yves European Journal of Organic Chemistry, 2002 , # 1 p. 105 - 111]
[Amatore, Muriel; Gosmini, Corinne Synlett, 2009 , # 7 p. 1073 - 1076]
[de Vries, Andre H. M.; Mulders, Jan M. C. A.; Mommers, John H. M.; Henderickx, Huub J. W.; de Vries, Johannes G. Organic Letters, 2003 , vol. 5, # 18 p. 3285 - 3288]
[Berthiol, Florian; Doucet, Henri; Santelli, Maurice Tetrahedron, 2006 , vol. 62, # 18 p. 4372 - 4383]
A Study of the Reaction of OH radical with CO by Time-resolved FTIR Spectroscopy
[Huang, Yixiang; Wang, Pingping; Liu, Jiaqin; Cai, Mingzhong Journal of Chemical Research, 2013 , vol. 37, # 6 p. 333 - 336]