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Bleeke, J. R.; Donnay, E.; Rath, N. P. Organometallics 2002, 21, 4099-4112
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For azapentadienyl-metal-phosphine complexes, see
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For phosphapentadienyl-metal-phosphine complexes, see
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For phosphapentadienyl-metal-phosphine complexes, see: Bleeke, J. R.; Rohde, A. M.; Robinson, K. D. Organometallics 1995, 14, 1674-1680
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For silapentadienyl-metal-phosphine complexes, see
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For silapentadienyl-metal-phosphine complexes, see: Bleeke, J. R.; Thananatthanachon, T.; Rath, N. P. Organometallics 2008, 27, 2436-2446
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Bleeke, J. R.; Lutes, B. L.; Rath, N. P. Organometallics 2009, 28, 4577-4583
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0000531567
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For synthesis of the analogous Li salt, see
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For synthesis of the analogous Li salt, see: Wolf, G.; Wurthwein, E.-U. Chem. Ber. 1991, 124, 889-896
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Alternatively, a Berry pseudorotation may be responsible, but the small "bite angle" of the allyl moiety makes this pathway more strained and, in our view, less likely. See
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Alternatively, a Berry pseudorotation may be responsible, but the small "bite angle" of the allyl moiety makes this pathway more strained and, in our view, less likely. See: Albright, T. A.; Hofmann, P.; Hoffmann, R. J. Am. Chem. Soc. 1977, 99, 7546-7557
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1 isomerizations are common in allyl-metal chemistry: University Science Books: Mill Valley, CA
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1 isomerizations are common in allyl-metal chemistry: Collman, J. P.; Hegedus, L. S.; Norton, J. R.; Finke, R. G. Principles and Applications of Organotransition Metal Chemistry; University Science Books: Mill Valley, CA, 1987; pp 175-181.
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MiTeGen, LLC, PO Box 3867, Ithaca, NY, 14852.
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MiTeGen, LLC, PO Box 3867, Ithaca, NY, 14852.
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