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3: (d) Dessolin, M.; Guillerez, M.G.; Thieriet, N.; Guibé, F.; Loffet, A. Tetrahedron Lett. 1995, 36, 5741. For palladium-catalyzed allyl cleavage under acidic conditions, see: (e) Smith, A. B., III; Rivero, R. A.; Hale, K. J.; Vaccaro, H. A. J. Am. Chem. Soc. 1991, 113, 2092. (f) Nakayama, K.; Uoto, K.; Higashi, K.; Soga, T.; Kusama, T. Chem. Pharm. Bull. 1992, 40, 1718. (g) In our methodology, we presume that carbonate anion acts as the nucleophile to react with the Pd-π-allyl species. However, note that this claim is unsubstantiated at this time.
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0348085945
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note
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When this reaction was carried out in ethanol, the corresponding deprotected ethyl ester was obtained as the only product. See also Table 1, entry 7.
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