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The organic chemistry of palladacycles has been reviewed: A. D. Ryabov, Synthesis 1985, 233.
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15744367494
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note
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-3). Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-179-85. Copies of the data can be obtained free of charge on application to the Director, CCDC, 12 Union Road, GB-Cambridge CB21EZ (UK) (Fax: Int. code +(1223) 336-033; e-mail: teched@chemcrys.cam.ac.uk).
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0001778618
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a) N. N. Lyalina, S. V. Dargina, A. N. Sobolev, T. M. Buslaeva, I. P. Romm, Koord. Khim. 1993, 19, 57;
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Lyalina, N.N.1
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23
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0000461962
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We have previously shown that intermediate 4 is consistent with kinetic data for oxidative addition of aryl halides to 2: J. F. Hartwig, F. Paul, J. Am. Chem. Soc. 1995, 117, 5373.
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Hartwig, J.F.1
Paul, F.2
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24
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note
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We have observed some formation of Suzuki coupling products with pure catalyst 1, but have not enjoyed the same high turnover numbers observed by the authors of reference [5], despite observation of Suzuki products in high yields with 2. Thus, our studies focus on Stille chemistry that gives high yields in our hands.
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