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[1]
Miyaura, N.; Yamada, K.; Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett., 1979, 20(36), 3437-3440.
[http://dx.doi.org/10.1016/S0040-4039(01)95429-2]
[http://dx.doi.org/10.1016/S0040-4039(01)95429-2]
[2]
Magano, J.; Dunetz, J.R. Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals. Chem. Rev., 2011, 111(3), 2177-2250.
[http://dx.doi.org/10.1021/cr100346g] [PMID: 21391570]
[http://dx.doi.org/10.1021/cr100346g] [PMID: 21391570]
[3]
Biajoli, A.F.P.; Schwalm, C.S.; Limberger, J.; Claudino, T.S.; Monteiro, A.L. Recent progress in the use of Pd-catalyzed C-C cross-coupling reactions in the synthesis of pharmaceutical compounds. J. Braz. Chem. Soc., 2011, 25(12), 2186-2214.
[4]
Li, H.; Johansson Seechurn, C.C.C.; Colaco, T.J. Development of preformed Pd catalysts for cross-coupling reactions, beyond the 2010 Nobel prize. ACS Catal., 2010, 2(6), 1147-1164.
[http://dx.doi.org/10.1021/cs300082f]
[http://dx.doi.org/10.1021/cs300082f]
[5]
Rao, G.K.; Kumar, A.; Ahmed, J.; Singh, A.K. Palladacycle containing nitrogen and selenium: highly active pre-catalyst for the Suzuki-Miyaura coupling reaction and unprecedented conversion into nano-sized Pd17Se15. Chem. Commun. (Camb.), 2010, 46(32), 5954-5956.
[http://dx.doi.org/10.1039/c0cc01075h] [PMID: 20625588]
[http://dx.doi.org/10.1039/c0cc01075h] [PMID: 20625588]
[6]
Kumar, A.; Rao, G.K.; Kumar, S.; Singh, A.K. Formation and role of palladium chalcogenide and other species in Suzuki–Miyaura and Heck C–C
coupling reactions catalyzed with palladium(II) complexes of organochalcogen ligands: Realities and speculations. Organometallics,. 2014, 33(12), 2921-2943.
[http://dx.doi.org/10.1021/om4007196]
[http://dx.doi.org/10.1021/om4007196]
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