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0032785772
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2(pybox- ip)[(-)-(E)-cyclooctene] (from 150.6 to 148.7 Hz); see: Similar changes for (±)- 4a, (±)- 4b, and their congeners will be measured and reported separately
-
2(pybox- ip)[(-)-(E)-cyclooctene] (from 150.6 to 148.7 Hz); see: Nishiyama, H.; Naitoh, T.; Motoyama, Y.; Aoki, K. Chem. Eur. J. 1999, 3509-3513 Similar changes for (±)- 4a, (±)- 4b, and their congeners will be measured and reported separately.
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Nishiyama, H.1
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50549102934
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Tsipis, A. C. Organometallics 2008, 27, 3701-3713 and references therein.
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Tsipis, A.C.1
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38
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78650652967
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3 solution, despite the unsymmetrical structure of their olefinic units (see the Supporting Information)
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3 solution, despite the unsymmetrical structure of their olefinic units (see the Supporting Information).
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-
39
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0012879192
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-
As early as 1969, Orchin and co-workers reported (14a) that pyridinic ligands undergo more rapid ligand exchange with solvent molecules than olefinic ligands in this class of compounds, but the anomalous feature of 3 arising from 2,6-disubstitution at the pyridine nuclei has been documented later by a number of research groups (3b-3f) including themselves. (14b)
-
As early as 1969, Orchin and co-workers reported (14a) that pyridinic ligands undergo more rapid ligand exchange with solvent molecules than olefinic ligands in this class of compounds, but the anomalous feature of 3 arising from 2,6-disubstitution at the pyridine nuclei has been documented later by a number of research groups (3b-3f) including themselves. (14b) Kaplan, P. D.; Schmidt, P.; Brause, A.; Orchin, M. J. Am. Chem. Soc. 1969, 91, 85-88
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Kaplan, P.D.1
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68949179036
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33947481315
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Evans, A.1
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44
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33847315130
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Tsuchiya, K.; Kondo, H.; Nagashima, H. Organometallics 2007, 26, 1044-1051 and references therein.
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Tsuchiya, K.1
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Nagashima, H.3
-
46
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78650653913
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The thermolysis of (±)- 4b in toluene at 80°C for 1.5 h resulted in its complete consumption to give a mixture, from which (±)- 6b was isolated in 54% yield
-
The thermolysis of (±)- 4b in toluene at 80°C for 1.5 h resulted in its complete consumption to give a mixture, from which (±)- 6b was isolated in 54% yield.
-
-
-
-
47
-
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78650642236
-
-
5, although similar reaction conditions have been very effective for the preparation of the series (±)- 1a - d
-
5, although similar reaction conditions have been very effective for the preparation of the series (±)- 1a - d.
-
-
-
-
48
-
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78650670800
-
-
1H} NMR data for the coordinated olefinic parts of (±)- 4ax, (±)- 4bx, (±)- 4ay, and (±)- 5a are compiled in the Supporting Information
-
1H} NMR data for the coordinated olefinic parts of (±)- 4ax, (±)- 4bx, (±)- 4ay, and (±)- 5a are compiled in the Supporting Information.
-
-
-
-
49
-
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78650643373
-
-
The solid-state structures of (±)- 4bx and (±)- 5a were also determined by X-ray diffraction. See the Supporting Information
-
The solid-state structures of (±)- 4bx and (±)- 5a were also determined by X-ray diffraction. See the Supporting Information.
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