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(a) Bäckvall, J. E. 'Stereocontrol in Palladium-Catalyzed Reactions', in: Bateson, J. H. and Mitchell, M. B., Eds., Organometallic Reagents in Organic Synthesis, Academic Press, London 1994, pp. 81-97
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When a carbon nucleophile was used in place of an oxygen nucleophile, the diene corresponding to 9 was isolated. In this case the diene is more stable due to the lower leaving-group ability of the carbon: Rönn, M. Unpublished results.
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For nucleophilic attack on (π-allyl) palladium complexes in DMSO see Tsuji, J., Takahashi, H. and Morikawa, N. Tetrahedron Lett. (1965) 4387. For nucleophilic attack on (π-allyl)palladium complexes with 1,4-benzoquinone as ligand see Bäckvall, J. E., Nordberg, R. E. and Wilhelm, D. J. Am. Chem. Soc. 107 (1985) 6892; Bäckvall, J. E. and Gogoll, A. Tetrahedron Lett. 29 (1988) 2243.
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For nucleophilic attack on (π-allyl) palladium complexes in DMSO see Tsuji, J., Takahashi, H. and Morikawa, N. Tetrahedron Lett. (1965) 4387. For nucleophilic attack on (π-allyl)palladium complexes with 1,4-benzoquinone as ligand see Bäckvall, J. E., Nordberg, R. E. and Wilhelm, D. J. Am. Chem. Soc. 107 (1985) 6892; Bäckvall, J. E. and Gogoll, A. Tetrahedron Lett. 29 (1988) 2243.
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For nucleophilic attack on (π-allyl) palladium complexes in DMSO see Tsuji, J., Takahashi, H. and Morikawa, N. Tetrahedron Lett. (1965) 4387. For nucleophilic attack on (π-allyl)palladium complexes with 1,4-benzoquinone as ligand see Bäckvall, J. E., Nordberg, R. E. and Wilhelm, D. J. Am. Chem. Soc. 107 (1985) 6892; Bäckvall, J. E. and Gogoll, A. Tetrahedron Lett. 29 (1988) 2243.
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