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1
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Reviews: (a) Gibson, D. H. Chem. Rev. 1996, 96, 2063.
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Gibson, D.H.1
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(b) Farina, V.; Krishnamurthy, V.; Scott, W. J. Org. React. 1997, 50, 1.
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Org. React.
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Farina, V.1
Krishnamurthy, V.2
Scott, W.J.3
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7
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33646315593
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note
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2 with 1,3-dienes and alkynes, which likely proceed via metal-carboxylate intermediates, often produce esters or lactones; for reviews and lead references, see ref 1c, pp 94-96 and 106-129.
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12
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0032971683
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Amatore, C.; Jutand, A.; Meyer, G.; Mother, L. Chem. Eur. J. 1999, 5, 466.
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Chem. Eur. J.
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Jutand, A.1
Meyer, G.2
Mother, L.3
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13
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33646318824
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note
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2 three times and then pressurized to 750 psig. The system was then heated at 70 °C for 48 h. After cooling, the autoclave was vented, the solvent was removed by rotary evaporation, and the ester products were isolated by Kugelrohr distillation. In some runs naphthalene was added as an internal standard; samples were withdrawn periodically via a dip tube and analyzed by GC. Spectroscopic data for ester 3a are included in the Supporting Information.
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14
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20444496149
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Pd-catalyzed aryltin-vinyl halide coupling (without carboxylation) has recently been achieved using supercritical carbon dioxide as solvent: Morita, D. K.; Pesiri, D. R.; David, S. A.; Glaze, W. H.; Tumas, W. J. Chem. Soc., Chem. Commun. 1998, 1397.
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J. Chem. Soc., Chem. Commun.
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Morita, D.K.1
Pesiri, D.R.2
David, S.A.3
Glaze, W.H.4
Tumas, W.5
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15
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0001289535
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(a) Henc, B.; Jolly, P. W.; Salz, R.; Wilke, G.; Benn, R.; Hoffman, E. G.; Mynott; R.; Schroth, G.; Seevogel, K.; Sekutowski, J. C.; Kruger, C. J. Organomet. Chem. 1980, 191, 425.
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J. Organomet. Chem.
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Henc, B.1
Jolly, P.W.2
Salz, R.3
Wilke, G.4
Benn, R.5
Hoffman, E.G.6
Mynott, R.7
Schroth, G.8
Seevogel, K.9
Sekutowski, J.C.10
Kruger, C.11
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16
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0000978596
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(b) Henc, B.; Jolly, P. W.; Salz, R.; Stobbe, S.; Wilke, G.; Bonn, R.; Mynott, R.; Seevogel, K.; Goddard, R.; Kruger, C. J. Organomet. Chem. 1980. 191, 449.
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J. Organomet. Chem.
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Henc, B.1
Jolly, P.W.2
Salz, R.3
Stobbe, S.4
Wilke, G.5
Bonn, R.6
Mynott, R.7
Seevogel, K.8
Goddard, R.9
Kruger, C.10
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17
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0038552751
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(a) Fitton, P.; Johnson, M. P.; McKeon, J. E. J. Chem. Soc., Chem. Commun. 1968, 6.
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J. Chem. Soc., Chem. Commun.
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Fitton, P.1
Johnson, M.P.2
McKeon, J.E.3
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19
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0008526782
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Cotton, F. A.; Faller, J. W.; Musco, A. Inorg. Chem. 1967, 6, 179.
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Inorg. Chem.
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Cotton, F.A.1
Faller, J.W.2
Musco, A.3
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20
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0029929193
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Nakamura, H.; Iwama, H.; Yamamoto, Y. J. Am. Chem. Soc. 1996, 118, 6641.
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Nakamura, H.1
Iwama, H.2
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22
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33646313706
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Dissertation, Ruhr-Universitat, Bochum, Germany
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(b) Hung, T. Dissertation, Ruhr-Universitat, Bochum, Germany, 1980.
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Hung, T.1
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24
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85016542275
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Ito, T.; Kindaichi, Y.; Takami, Y. Chem. Ind. (London) 1980, 19, 83.
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Chem. Ind. (London)
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Ito, T.1
Kindaichi, Y.2
Takami, Y.3
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25
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0030755285
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A similar scheme has been proposed for the recently reported Pd-catalyzed three-component coupling of allylstannanes, allyl halides, and electrophilic alkenes: Nakamura, H.; Shim, J.-G.; Yamamoto, Y. J. Am. Chem. Soc. 1997, 119, 8113.
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(1997)
J. Am. Chem. Soc.
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Nakamura, H.1
Shim, J.-G.2
Yamamoto, Y.3
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26
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0345152496
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3: Christofides, A.; Ciriano, M.; Spencer, J. L.; Stone, F. G. A. J. Organomet. Chem. 1979, 178, 273.
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Christofides, A.1
Ciriano, M.2
Spencer, J.L.3
Stone, F.G.A.4
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27
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33646284570
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note
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119Sn NMR spectra with those of authentic samples.
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28
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33646324923
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note
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The identities of esters 3a-d were established by GC/MS and NMR analysis of the mixture and by comparison with authentic samples of each ester, which were prepared by DCC-DMAP-promoted reactions of the respective carboxylic acids and alcohols. Spectral data for 3a-d are available in the Supporting Information.
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