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For representative papers on polymer-supported phosphine-palladium complex, see:
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For representative papers on polymer-supported phosphine-palladium complex, see:. Parrish C.A., and Buchwald S.L. J. Org. Chem. 66 (2001) 3820
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Porco Jr., J.A.3
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For representative papers on polymer-supported N-heterocyclic carbene-palladium complexes, see:
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For representative papers on polymer-supported N-heterocyclic carbene-palladium complexes, see:. Byun J.-W., and Lee Y.-S. Tetrahedron Lett. 45 (2004) 1837
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For representative papers on polymer-supported salen-palladium complexes and others, see:
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For representative papers on polymer-supported salen-palladium complexes and others, see:. Phan N.T.S., Brown D.H., and Styring P. Tetrahedron Lett. 45 (2004) 7915
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For representative papers on others polymer-supported palladium complexes, see:
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For representative papers on others polymer-supported palladium complexes, see:. Lau K.C.Y., He H.S., Chiu P., and Toy P.H. J. Comb. Chem. 6 (2004) 955
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For selected recent papers on the palladium-catalyzed Suzuki-Miyaura cross-couplings to construct heteroaryl-aryls, see:
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For selected recent papers on the palladium-catalyzed Suzuki-Miyaura cross-couplings to construct heteroaryl-aryls, see:. Molander G.A., and Biolatto B. J. Org. Chem. 68 (2003) 4302
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Guram A.S., King A.O., Allen J.G., Wang X., Schenkel L.B., Chan J., Bunel E.E., Faul M.M., Larsen R.D., Martinelli M.J., and Reider P.J. Org. Lett. 8 (2006) 1787
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46
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4344643818
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2-catalyzed Suzuki-Miyaura cross-coupling reaction, see:
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2-catalyzed Suzuki-Miyaura cross-coupling reaction, see:. Li J.-H., and Liu W.-J. Org. Lett. 6 (2004) 2809
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Li, J.-H.1
Liu, W.-J.2
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33751282815
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note
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4 (0.25 mL)].
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50
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33751272074
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note
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2OH).
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33751300929
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note
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The loading level of Pd was decreased to 0.039 mmol/g after the fifth run, which was calculated by ICP-AES.
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