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Bolm, C.1
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a) Review on asymmetric allylic substitutions: B. M. Trost, M. L. Crawley, Chem. Rev. 2003, 103, 2921;
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Trost, B.M.1
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a) A. Leitner, S. Shekhar, M. J. Pouy, J. F. Hartwig, J. Am. Chem. Soc. 2005, 127, 15506;
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Leitner, A.1
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17444425377
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and references therein
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b) C. Welter, A. Dahnz, B. Brunner, S. Streiff, P. Dübon, G. Helmchen, Org. Lett. 2005, 7, 1239, and references therein.
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Welter, C.1
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a) R. Hermatschweiler, I. Fernandez, F. Breher, P. S. Pregosin, L. F. Veiros, M. J. Calhorda, Angew. Chem. 2005, 117, 4471;
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b) R. Hermatschweiler, I. Fernandez, P. S. Pregosin, E. J. Watson, A. Albinati, S. Rizzato, L. F. Veiros, M. J. Calhorda, Organometallics 2005, 24, 1809.
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Organometallics
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14
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77955911241
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(Ed.: P. A. Evans), Wiley-VCH, Weinheim
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a) Review on rhodium-catalyzed allylic substitutions: D. K. Leahy, P. A. Evans in Modern Rhodium-Catalyzed Organic Reactions (Ed.: P. A. Evans), Wiley-VCH, Weinheim, 2005, p. 191;
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Modern Rhodium-Catalyzed Organic Reactions
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Leahy, D.K.1
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b) P. A. Evans, J. E. Robinson, K. K. Moffett, Org. Lett. 2001, 3, 3269;
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d) P. A. Evans, J. E. Robinson, J. D. Nelson, J. Am. Chem. Soc. 1999, 121, 6761.
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19
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33748803771
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note
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"Direct nucleophiles" are distinguished by the fact that the nucleophilic center does not have to be activated prior to the reaction (through, for example, deprotonation).
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20
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0030968870
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and references therein
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Oxidative, iron-catalyzed aminations of unactivated olefins: R. S. Srivastava, K. M. Nicholas, J. Am. Chem. Soc. 1997, 119, 3302, and references therein.
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Srivastava, R.S.1
Nicholas, K.M.2
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21
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0037978732
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For a common reaction between iron carbonyl complexes and nitrogen bases, see: a) W. Hieber, N. Kahlen, Chem. Ber. 1958, 91, 2223;
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Chem. Ber.
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Hieber, W.1
Kahlen, N.2
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23
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0032416884
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[8] The electronic influence of various substituents on conversion and yield in the stoichiometric amination of π-allyl iron complexes has been described: S. Nakanishi, K. Okamoto, H. Yamaguchi, T. Takata, Synthesis 1998, 1735.
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Synthesis
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Nakanishi, S.1
Okamoto, K.2
Yamaguchi, H.3
Takata, T.4
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24
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2542504340
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The only broadly applicable procedure for the allylic substitution of higher-substituted allyl carbonates by the mechanism involving a σ-allyl metal fragment to be reported so far was published by Martin et al.: B. L. Ashfeld, K. A. Miller, S. F. Martin, Org. Lett. 2004, 6, 1321.
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Org. Lett.
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Ashfeld, B.L.1
Miller, K.A.2
Martin, S.F.3
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