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Communicated in part at ISHHC-XI, July 21-25, 2003, Evanston, IL, Poster Abstract No. 034
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Communicated in part at ISHHC-XI, July 21-25, 2003, Evanston, IL, Poster Abstract No. 034.
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See Supporting Information for complete details
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See Supporting Information for complete details.
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39
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33845282603
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For examples of μ-halide crystal structures, see: (a) Evans, W. J.; Drummond, D. K.; Grate, J. W.; Zhang, H.; Atwood, J. L. J. Am. Chem. Soc, 1987, 109 (13), 3928-3936.
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41
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0345273520
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note
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Single crystals suitable for X-ray diffraction studies have not been obtained to date, although NMR spectroscopy, electron-impact mass spectrometry, and elemental analysis indicate clean formation of 3 and 4 by this method.
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42
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(a) Fendrick, C. M.; Mintz, E. A.; Schertz, L. D.; Marks, T. J.; Day, V. W. Organometallics 1984, 3, 819.
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0035956453
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and references therein
-
For previously reported studies of organoactinide-mediated intermolecular terminal alkyne hydroamination, see: Straub, T.; Haskel, A.; Neyroud, T. G.; Kapon, M.; Botoshansky, M.; Eisen, M. S. Organometallics 2001, 20 (24), 5017-5035, and references therein.
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Eisen, M.S.6
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48
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0344842107
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note
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An alternative cycle proceeding through an An=NR species (see ref 18) as a catalytically inactive species or as the active catalyst species cannot be rigorously ruled out at this time. Imide formation as a reversible, turnover-limiting step seems unlikely given the observed independence of overall rate on [substrate].
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