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1
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For a review of metal-catalyzed Suzuki cross-coupling reactions, see: (a)
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For a review of metal-catalyzed Suzuki cross-coupling reactions, see: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483.
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(b) Diederich, F; Stang, P., Eds.; Wiley-VCH: Weiheim, Germany, Chapter 2
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(b) Suzuki, A. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F; Stang, P., Eds.; Wiley-VCH: Weiheim, Germany, 1998; Chapter 2.
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For recent palladium-based catalyzed couplings of arylchlorides, see: (a)
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For recent palladium-based catalyzed couplings of arylchlorides, see: (a) Hamann, B. C.; Hartwig, J. F. J. Am. Chem. Soc. 1998, 120, 7369-7370.
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(b)
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(b) Reetz, M. T.; Lohmer, G.; Schwickardi, R. Angew. Chem., Int. Ed. Engl. 1998, 37, 481-483.
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Reetz, M.T.1
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(c)
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(c) Bei, X.; Guram, A. S.; Turner, H. W.; Weinberg, W. H. Tetrahedron Lett. 1999, 40, 1237-1240.
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(d)
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(d) Littke, A. F.; Fu, G. C. Angew. Chem., Int. Ed. Engl. 1999, 38, 2411-2413.
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(a)
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(a) Old, D. W.; Wolfe, J. P.; Buchwald, S. L. J. Am. Chem. Soc. 1998, 120, 9722-9723.
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(b) Wolfe, J. P.; Buchwald, S. L. Angew. Chem., Int. Ed. Engl. 1999, 38, 2413-2415.
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Littke, A. F.; Fu, G. C. Angew. Chem., Int. Ed. Engl. 1998, 37, 3387-3388.
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(a) Bei X.; Crevier T.; Guram A.S.; Jandeleit B.; Powers T.S.; Turner H.W.; Uno T.; Weinberg W.H.
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(a) Bei, X.; Crevier, T.; Guram, A. S.; Jandeleit, B.; Powers, T. S.; Turner, H. W.; Uno, T.; Weinberg, W. H. Tetrahedron Lett. 1999, 40, 3855-3858.
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(b) Bei, X.; Turner, H. W.; Weinberg, W. H.; Guram, A. S.; Peterson, J. L. J. Org. Chem. 1999, 64, 6797-6803.
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(b) Hermann, W. A.; Köcher, C. Angew. Chem,. Int. Ed. Engl. 1997, 36, 2163-2187.
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0343222664
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3 (2.0 mmol) in dry dioxane (3 mL) at 80°C under argon for a 30 min catalyst activation period, followed by the addition of the aryl chloride (1.0 mmol) and the arylboronic acid (1.5 mmol)
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3 (2.0 mmol) in dry dioxane (3 mL) at 80°C under argon for a 30 min catalyst activation period, followed by the addition of the aryl chloride (1.0 mmol) and the arylboronic acid (1.5 mmol).
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