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Albrecht, M.1
van Koten, G.2
-
18
-
-
34547790514
-
-
See Supporting Information
-
See Supporting Information.
-
-
-
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19
-
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0003814053
-
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Diehl, P, Fluck, E, Eds, Springer-Verlag: New York
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Pregosin, P.S.1
Kunz, R.W.2
-
20
-
-
34547765653
-
-
PtAr = 636 Hz).
-
PtAr = 636 Hz).
-
-
-
-
21
-
-
34547737679
-
-
13C coupling constant of the aryl carbon in 3 is 1014 Hz, indicative of the very weak triflate trans to the aryl group.
-
13C coupling constant of the aryl carbon in 3 is 1014 Hz, indicative of the very weak triflate trans to the aryl group.
-
-
-
-
22
-
-
34547730487
-
-
3 by GC/MS.
-
3 by GC/MS.
-
-
-
-
23
-
-
33845554618
-
-
(a) Grove, D. M.; van Koten, G.; Louwen, J. N.; Noltes, J. G.; Spek, A. L.; Ubbels, H. J. C. J. Am. Chem. Soc. 1982, 104, 6609.
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Grove, D.M.1
van Koten, G.2
Louwen, J.N.3
Noltes, J.G.4
Spek, A.L.5
Ubbels, H.J.C.6
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24
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0034838171
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(b) Albrecht, M.; Spek, A. L.; van Koten, G. J. Am. Chem. Soc. 2001, 123, 7233.
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Albrecht, M.1
Spek, A.L.2
van Koten, G.3
-
26
-
-
34547780245
-
-
See Supporting Information for details
-
See Supporting Information for details.
-
-
-
-
27
-
-
34547784238
-
-
An alternate mechanism in which the Pt-bound CH3 group itself acts as the nucleophile cannot be conclusively ruled out, though it lacks the precedent of an oxidative addition-type pathway ref 23 and references therein
-
3 group itself acts as the nucleophile cannot be conclusively ruled out, though it lacks the precedent of an oxidative addition-type pathway (ref 23 and references therein).
-
-
-
-
28
-
-
0034806687
-
-
(a) Fekl, U.; Kaminsky, W.; Goldberg, K. I. J. Am. Chem. Soc. 2001, 123, 6423.
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Fekl, U.1
Kaminsky, W.2
Goldberg, K.I.3
-
30
-
-
34547797129
-
-
3 (the latter of which was observed by NMR and GC/MS).
-
3 (the latter of which was observed by NMR and GC/MS).
-
-
-
-
31
-
-
34547804516
-
-
2H NMR spectroscopies.
-
2H NMR spectroscopies.
-
-
-
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