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Hassan, J.1
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Gozzi, C.3
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Lemaire, M.5
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84994387666
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Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: Weinheim, Chapter 2
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(b) Suzuki, A. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F.; Stang, P. J., Eds.; Wiley-VCH: Weinheim, 1998; Chapter 2;
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Suzuki, A.1
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Miyaura, N.1
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Wong T.-K., Chien Y.-Y., Liao Y.-L., Lin C.-C., Chou M.-Y., Leung M.-k. J. Org. Chem. 67:2002;1041-1044.
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Wong, T.-K.1
Chien, Y.-Y.2
Liao, Y.-L.3
Lin, C.-C.4
Chou, M.-Y.5
Leung, M.-K.6
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0037178508
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Li W., Nelson D.P., Jensen M.S., Hoerrner R.S., Cai D., Larsen R.D., Reider P.J. J. Org. Chem. 67:2002;5394-5397.
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Li, W.1
Nelson, D.P.2
Jensen, M.S.3
Hoerrner, R.S.4
Cai, D.5
Larsen, R.D.6
Reider, P.J.7
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11
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0037182035
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Bouillon A., Lancelot J.-C., Collot V., Bovy P.R., Rault S. Tetrahedron. 58:2002;4369-4373.
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Tetrahedron
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Bouillon A., Lancelot J.-C., Collot V., Bovy P.R., Rault S. Tetrahedron. 58:2002;3323-3328.
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Collot, V.3
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Rault, S.5
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16
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0030035796
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Fernando S.R.L., Maharoof U.S.M., Deshayes K.D., Kinstle T.H., Ogawa M.Y. J. Am. Chem. Soc. 118:1996;5783-5790.
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Fernando, S.R.L.1
Maharoof, U.S.M.2
Deshayes, K.D.3
Kinstle, T.H.4
Ogawa, M.Y.5
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19
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84994407272
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All reaction products and starting materials are commercially available. The calibration curves to determine relative reponses by flame-ionization detection were generated using commercial chemicals of at least 98% purity. A reaction that indicated a GC yield of 79% 2,2′-bipyridine (16) afforded a purified yield of 73% after column chromatography
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All reaction products and starting materials are commercially available. The calibration curves to determine relative reponses by flame-ionization detection were generated using commercial chemicals of at least 98% purity. A reaction that indicated a GC yield of 79% 2,2′-bipyridine (16) afforded a purified yield of 73% after column chromatography.
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22
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84994407298
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2 (35 mg, 0.05 mmol), and biphenyl (50 mg) were dissolved in solvent (10 mL) in a 20 mL scintillation vial equipped with a stir bar. No precautions were taken to exclude atmospheric oxygen. The vial was sealed and heated to 100°C. The reaction was periodically monitored by GC to determine extent of reaction relative to the size of the biphenyl internal standard peak
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2 (35 mg, 0.05 mmol), and biphenyl (50 mg) were dissolved in solvent (10 mL) in a 20 mL scintillation vial equipped with a stir bar. No precautions were taken to exclude atmospheric oxygen. The vial was sealed and heated to 100°C. The reaction was periodically monitored by GC to determine extent of reaction relative to the size of the biphenyl internal standard peak.
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25
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84994469617
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Compound 29 is not commercially available. The GC response factor for this compound relative to biphenyl was approximated by taking the average of the response factors of 16 and 26
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Compound 29 is not commercially available. The GC response factor for this compound relative to biphenyl was approximated by taking the average of the response factors of 16 and 26.
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