Palladium-catalyzed reductive coupling of styrenes and organostannanes under aerobic conditions

KM Gligorich, SA Cummings…

Index: Gligorich, Keith M.; Cummings, Sarah A.; Sigman, Matthew S. Journal of the American Chemical Society, 2007 , vol. 129, # 46 p. 14193 - 14195

Full Text: HTML

Citation Number: 46

Abstract

We report a highly regioselective PdII-catalyzed reductive coupling of an alkene with an organostannane using a tandem alcohol oxidation under aerobic conditions. Both aryl-and vinylstannanes are competent coupling partners with a variety of styrene derivatives. Mechanistic experiments support a tandem alcohol oxidation/alkene functionalization process. The ability to trap a palladium hydride derived from alcohol oxidation with an ...

Related Articles:

Total synthesis of ovalifoliolatin B, acerogenins A and C

[Kishore Kumar; Natarajan, Amarnath Tetrahedron Letters, 2008 , vol. 49, # 13 p. 2103 - 2105]

Enantioselective synthesis of (R)-phenylephrine hydrochloride

[Pandey, Rajesh Kumar; Upadhyay, Puspesh Kumar; Kumar, Pradeep Tetrahedron Letters, 2003 , vol. 44, # 33 p. 6245 - 6246]

Enantioselective synthesis of (R)-phenylephrine hydrochloride

[Pandey, Rajesh Kumar; Upadhyay, Puspesh Kumar; Kumar, Pradeep Tetrahedron Letters, 2003 , vol. 44, # 33 p. 6245 - 6246]

Enantioselective synthesis of (R)-phenylephrine hydrochloride

[Pandey, Rajesh Kumar; Upadhyay, Puspesh Kumar; Kumar, Pradeep Tetrahedron Letters, 2003 , vol. 44, # 33 p. 6245 - 6246]

More Articles...