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0442270527
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note
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- was employed as the catalyst. The individual precatalysls employed separately gave no cyclization under reaction conditions.
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34
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33748495564
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Hill, G. S.; Rendina, L. M.; Puddephatt, R. J. J. Chem. Soc., Dalton Trans. 1996, 1809.
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35
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0442302068
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note
-
These catalysis were inactive toward both dienes and enynes.
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-
-
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36
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0442317559
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note
-
Addition of toluene to the precatalyst mixture prior to the diyne led to immediate darkening of the solution and low subsequent conversion. This observation suggests that the cationic platinum complex formed via methyl abstraction is unstable in the absence ot a coordinating ligand such as an alkyne.
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37
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0442270509
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note
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1H NOE. The remainder of the products consisted of disilylated compounds.
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42
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0034301849
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19b complexes has been demonstrated. (a) Pfeiffer, J.; Kickelbick, G.; Schubert, U. Organometallics 2000, 19, 61 (b) Fang, X.; Scott, B. L.; Watkins, J. G.; Kubas, G. J. Organometallics 2000, 19, 4193.
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Pfeiffer, J.1
Kickelbick, G.2
Schubert, U.3
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43
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0034301849
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19b complexes has been demonstrated. (a) Pfeiffer, J.; Kickelbick, G.; Schubert, U. Organometallics 2000, 19, 61 (b) Fang, X.; Scott, B. L.; Watkins, J. G.; Kubas, G. J. Organometallics 2000, 19, 4193.
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Fang, X.1
Scott, B.L.2
Watkins, J.G.3
Kubas, G.J.4
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44
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0442270528
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note
-
Diyne 1 could also enter the catalytic cycle in the conversion of II to III. Initial formation of I presumably occurs via H-Si oxidative addition to a cationic Pt-Me complex followed by C-H reductive elimination.
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45
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0442317560
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note
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2 led to diminished yield.
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