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(a) Review for allylic amination: Johannsen, M.; Jørgensen, K. A. Chem. Rev. 1998, 98, 1689. (b) Muchow, G.; Brunel, J. M.; Maffei, M.; Pardigon, O.; Buono, G. Tetrahedron 1998, 54, 10435.
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(1998)
Tetrahedron
, vol.54
, pp. 10435
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Muchow, G.1
Brunel, J.M.2
Maffei, M.3
Pardigon, O.4
Buono, G.5
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81
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0001925439
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(b) Lindner, E.; Wang, Q.; Mayer, H. A.; Fawzi, R.; Steimann, M. J. Organomet. Chem. 1993, 453, 289.
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(1993)
J. Organomet. Chem.
, vol.453
, pp. 289
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Lindner, E.1
Wang, Q.2
Mayer, H.A.3
Fawzi, R.4
Steimann, M.5
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83
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0000372412
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(d) Brown, J. M.; Cook, S. J.; Kent, A. G. Tetrahedron 1986, 42, 5097.
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(1986)
Tetrahedron
, vol.42
, pp. 5097
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Brown, J.M.1
Cook, S.J.2
Kent, A.G.3
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84
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0000542088
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(e) Lindner, E.; Wang, Q.; Mayer, H. A.; Fawzi, R.; Steimann, M. Organometallics 1993, 12, 1865.
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(1993)
Organometallics
, vol.12
, pp. 1865
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Lindner, E.1
Wang, Q.2
Mayer, H.A.3
Fawzi, R.4
Steimann, M.5
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85
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0345225100
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note
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3, F(000) = 2152, 4998 Independent reflections with I/σ(I) 2.0 were used on the analysis. Data for crystallographic analysis were measured on an Enraf-Nonius CAD-4 diffractormeter using graphite-monochromate MoKα (λ = 0.710 73 Å) and ω-2 scans in the range of θ; 1.36 < θ < 25.35. Structure was solved by direct methods and refined by least squares using the SHEL-X.
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86
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0031017921
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2+ where R = Ph and cyclohexyl, have been recently reported. See Allgeier, A.; Slone, C. S.; Mirkin, C. A.; Liable-Sands, L. M.; Yap, G. P. A.; Rheingold, A. L. J. Am. Chem. Soc. 1997, 119, 550.
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(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 550
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Allgeier, A.1
Slone, C.S.2
Mirkin, C.A.3
Liable-Sands, L.M.4
Yap, G.P.A.5
Rheingold, A.L.6
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