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17
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5244236866
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note
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References 7-12 provide logical groupings of our studies of adducts of I and nitrogen donor ligands.
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18
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(a) Knight, D. A.; Dewey, M. A.; Stark, G. A.; Bennett, B. K.; Arif, A. M.; Gladysz, J. A. Organometallics 1993, 12, 4523.
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(b) Stark, G. A.; Arif, A. M.; Gladysz, J. A. Organometallics 1994, 13, 4523.
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(a) Johnson, T. J.; Arif, A. M.; Gladysz, J. A. Organometallics 1994, 13, 3182.
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39
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0000218987
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For other types of complexes with MNLi linkages, see: (a) Glassman, T. E.; Vale, M. G.; Schrock, R. R. Organometallics 1991, 10, 4046. (b) Pérez, P. J.; Luan, L.; White, P. S.; Brookhart, M.; Templeton, J. L. J. Am. Chem. Soc. 1992, 114, 7928.
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0642366347
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For other types of complexes with MNLi linkages, see: (a) Glassman, T. E.; Vale, M. G.; Schrock, R. R. Organometallics 1991, 10, 4046. (b) Pérez, P. J.; Luan, L.; White, P. S.; Brookhart, M.; Templeton, J. L. J. Am. Chem. Soc. 1992, 114, 7928.
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41
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5244309449
-
-
note
-
All diastereomer and enantiomer ratios are normalized to 100. For NMR determinations, error limits on each component are generally ±2. When no signal can be detected for a second, independently prepared isomer, a ≥99:≤1 ratio is assumed.
-
-
-
-
42
-
-
5244313329
-
-
note
-
7,10,14b and are specified prior to carbon configurations. Serendipitously, R/S designations also track the relative configurations for all compounds in this paper.
-
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43
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0011581170
-
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2 in thermostated cells utilizing procedures described earlier: Dewey, M. A.; Gladysz, J. A. Organometallics 1993, 12, 2390.
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5244264553
-
-
note
-
The preparative yield of this spectroscopically quantitative transformation was not optimized.
-
-
-
-
47
-
-
5244281624
-
-
note
-
19 were adjusted by up to ±2 (the experimental error) to optimize linearity.
-
-
-
-
48
-
-
5244363232
-
-
note
-
t vs time plots.
-
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49
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0003604511
-
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Wiley: New York
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‡ values were estimated according to: Wiberg, K. B. Physical Organic Chemistry; Wiley: New York, 1964; pp 378-379.
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3 at 10 °C, and initial cyclopentadienyl ligand slippage has been proposed: Glueck, D. S.; Bergman, R. G. Organometallics 1991, 10, 1479.
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(b) For leading references and comparisons of β-hydride eliminations in coordinatively unsaturated iridium amido, alkoxide, and alkyl complexes, see: Hartwig, J. F. J. Am. Chem. Soc. 1996, 118, 7010.
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Agbossou, S.K.1
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75
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5244379060
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note
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- (text and Scheme 1) were conducted analogously to those described in the epimerization experiments.
-
-
-
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76
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5244248925
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note
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13C) values unless noted and are in Hz. For samples that are mixtures of diastereomers. paired resonances are separated by slashes (/).
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