Regioselective palladium-catalyzed arylation of 2-furaldehyde
…, B Glover, E McSorley, A Millar, MH Osterhout…
Index: McClure; Glover; McSorley; Millar; Osterhout; Roschangar Organic letters, 2001 , vol. 3, # 11 p. 1677 - 1680
Full Text: HTML
Citation Number: 122
Abstract
An efficient regioselective method for the direct arylation of 2-furaldehyde to provide a range of π-diverse 5-aryl-2-formylfuran derivatives is described. The method employs functionalized aryl halides and a catalytic amount of palladium (II) chloride under relatively mild conditions.
Related Articles:
[Feuerstein, Marie; Doucet, Henri; Santelli, Maurice Journal of Organometallic Chemistry, 2003 , vol. 687, # 2 p. 327 - 336]
A practical one-pot synthesis of 5-aryl-2-furaldehydes
[McClure; Roschangar; Hodson; Millar; Osterhout Synthesis, 2001 , # 11 p. 1681 - 1685]
[Hosoya, Takamitsu; Aoyama, Hiroshi; Ikemoto, Takaaki; Kihara, Yasutaka; Hiramatsu, Toshiyuki; Endo, Makoto; Suzuki, Masaaki Bioorganic and Medicinal Chemistry, 2003 , vol. 11, # 5 p. 663 - 673]
Synthesis of 5-pyridyl-2-furaldehydes via palladium-catalyzed cross-coupling with triorganozincates
[Gauthier Jr., Donald R.; Szumigala Jr., Ronald H.; Dormer, Peter G.; Armstrong III, Joseph D.; Volante; Reider, Paul J. Organic Letters, 2002 , vol. 4, # 3 p. 375 - 378]
A practical one-pot synthesis of 5-aryl-2-furaldehydes
[McClure; Roschangar; Hodson; Millar; Osterhout Synthesis, 2001 , # 11 p. 1681 - 1685]