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note
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a value is that of the conjugate acid of 2-ethylthiazole.
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43
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0001827606
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Wilkinson, G., Ed.; Pergamon Press: Oxford, UK
-
a value is that of the conjugate acid of 1-methylpyrazole. Reedijk, J. In Comprehensive Coordination Chemistry; Wilkinson, G., Ed.; Pergamon Press: Oxford, UK, 1987; Vol. 2, p 73.
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(1987)
Comprehensive Coordination Chemistry
, vol.2
, pp. 73
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Reedijk, J.1
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44
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3042759470
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note
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All compounds were characterized by NMR, IR, and mass spectral data. For new compounds, elemental analyses or high-resolution mass were measured. For full characterization of new compounds, see the Supporting Information.
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45
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3042831443
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a value is that of the conjugate acid of 1-methyl-1,2,4-triazole. Kroeger, C. F.; Freiberg, W. Chimia 1967, 21, 161.
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(1967)
Chimia
, vol.21
, pp. 161
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Kroeger, C.F.1
Freiberg, W.2
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46
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0036012172
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We recently found the transformation of C-H bonds to the C-Si bond by the Ru-catalyzed reaction of 8g with a hydrosilane at the benzylic position. Kakiuchi, F.; Igi, K.; Matsumoto, M.; Hayamizu, T.; Chatani, N.; Murai, S. Chem. Lett. 2002, 396. In the case of the carbonylation of 8g, the cleavage of the benzylic C-H bonds did not lead to the formation of carbonylation product, although we do not know the reason.
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(2002)
Chem. Lett.
, pp. 396
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Kakiuchi, F.1
Igi, K.2
Matsumoto, M.3
Hayamizu, T.4
Chatani, N.5
Murai, S.6
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47
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0001442962
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The mechanism of the formation of 9a is not clear. We have already obtained similar results, see ref 10a,c. There are two possible mechanisms for the formation of a protodesilylated product. One involves the formation of 9a by the reaction of 8a with CO and ethylene, which is formed, along with disilylethylene, from two molecules of vinylsilane via a Ru-catalyzed metathesis of vinylsilanes. For a paper on the ruthenium-catalyzed conversion of vinylsilane to ethylene and disilylethylene, see: Seki, Y.; Takeshita, K.; Kawamoto, K. J. Organomet. Chem. 1989, 369, 117. An alternative mechanism involves the hydrolysis of α-silyl ketone, a regioisomer of 19.
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(1989)
J. Organomet. Chem.
, vol.369
, pp. 117
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Seki, Y.1
Takeshita, K.2
Kawamoto, K.3
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48
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0000037108
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The mechanisms of carbon-heteroatom bond-forming reductive elimination of amines, ethers, and sulfides have recently been studied by Hartwig and Buchwald independently. The proposed mechanisms are stepwise mechanisms, which involve the inner-sphere attack of one ligand at the π-bond of the other ligand. Hartwig, J. F. Acc. Chem. Res. 1998, 31, 852. Widenhoefer, R. A.; Buchwald, S. L. J. Am. Chem. Soc. 1998, 120, 6504.
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(1998)
Acc. Chem. Res.
, vol.31
, pp. 852
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Hartwig, J.F.1
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49
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0032496933
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The mechanisms of carbon-heteroatom bond-forming reductive elimination of amines, ethers, and sulfides have recently been studied by Hartwig and Buchwald independently. The proposed mechanisms are stepwise mechanisms, which involve the inner-sphere attack of one ligand at the π-bond of the other ligand. Hartwig, J. F. Acc. Chem. Res. 1998, 31, 852. Widenhoefer, R. A.; Buchwald, S. L. J. Am. Chem. Soc. 1998, 120, 6504.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 6504
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Widenhoefer, R.A.1
Buchwald, S.L.2
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50
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0035821428
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Carrillo, J. R.; Cossío, F. P.; Díaz-Ortiz, A.; Gómez-Escalonilla, M. J.; de la Hoz, A.; Lecea, B.; Moreno, A.; Prieto, P. Tetrahedron 2001, 57, 4179. See also: Carrillo, J. R.; Cossio, F. P.; Diaz-Ortiz, A.; Gómez-Escalonilla, M. J.; de la Hoz, A.; Lecea, B.; Moreno, A.; Prieto, P. Tetrahedron 2001, 57, 4179.
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(2001)
Tetrahedron
, vol.57
, pp. 4179
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Carrillo, J.R.1
Cossío, F.P.2
Díaz-Ortiz, A.3
Gómez-Escalonilla, M.J.4
De La Hoz, A.5
Lecea, B.6
Moreno, A.7
Prieto, P.8
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51
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Carrillo, J. R.; Cossío, F. P.; Díaz-Ortiz, A.; Gómez-Escalonilla, M. J.; de la Hoz, A.; Lecea, B.; Moreno, A.; Prieto, P. Tetrahedron 2001, 57, 4179. See also: Carrillo, J. R.; Cossio, F. P.; Diaz-Ortiz, A.; Gómez-Escalonilla, M. J.; de la Hoz, A.; Lecea, B.; Moreno, A.; Prieto, P. Tetrahedron 2001, 57, 4179.
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(2001)
Tetrahedron
, vol.57
, pp. 4179
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Carrillo, J.R.1
Cossio, F.P.2
Diaz-Ortiz, A.3
Gómez-Escalonilla, M.J.4
De La Hoz, A.5
Lecea, B.6
Moreno, A.7
Prieto, P.8
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53
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0029147111
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Crowe, E.; Hossner, F.; Hughes, M. J. Tetrahedron 1995, 51, 8889. Prager, R. H.; Smith, J. A.; Weber, B.; Williams, C. M. J. Chem. Soc., Perkin Trans. 1 1997, 2665.
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(1995)
Tetrahedron
, vol.51
, pp. 8889
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Crowe, E.1
Hossner, F.2
Hughes, M.J.3
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54
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33748733257
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Crowe, E.; Hossner, F.; Hughes, M. J. Tetrahedron 1995, 51, 8889. Prager, R. H.; Smith, J. A.; Weber, B.; Williams, C. M. J. Chem. Soc., Perkin Trans. 1 1997, 2665.
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(1997)
J. Chem. Soc., Perkin Trans. 1
, pp. 2665
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Prager, R.H.1
Smith, J.A.2
Weber, B.3
Williams, C.M.4
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56
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0033595583
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Chatani, N.; Ie, Y.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 1999, 121, 8645.
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J. Am. Chem. Soc.
, vol.121
, pp. 8645
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Chatani, N.1
Ie, Y.2
Kakiuchi, F.3
Murai, S.4
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57
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3042836100
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note
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3 C-H bond, see ref 11b,c,e,g.
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58
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3042754808
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note
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In a pioneering study, Hong and Yamazaki reported on the Rh-catalyzed carbonylation of benzene, although the selectivity of products was quite low. See ref 2.
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