Efficient Method for β-Conjugate Addition of α, β-Unsaturated Lactones and Esters

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Posner, G. H. An Introduction to Synthesis Using OrganocopperReagents; Wiley-Interscience: New York, 1980.
Taylor, R.J. K. Organocopper Reagents; Oxford University Press: Oxford,1994.
Stowell, J. C. Chem. Rev. 1984, 84, 409. https://doi.org/10.1021/cr00063a001
Hoppe, D. Angew. Chem., Int. Ed. Engl. 1984, 23, 932. https://doi.org/10.1002/anie.198409321
Kozikowski, A. P.; Jung, S. H. J. Org. Chem. 1986, 51, 3400. https://doi.org/10.1021/jo00367a040
Kozikowski, A. P.; Jung, S. H. J. Tetrahedron Lett. 1986, 27,3227. https://doi.org/10.1016/S0040-4039(00)84760-7
Kim, S.; Lee, P. H. Tetrahedron Lett. 1988, 29, 5413. https://doi.org/10.1016/S0040-4039(00)82882-8
Kim,S.; Lee, P. H.; Kim, S. S. Bull. Korean Chem. Soc. 1989, 10, 218.
Kim, S.; Kim, Y. G.; Park, J. H. Tetrahedron Lett. 1991, 32,2043. https://doi.org/10.1016/S0040-4039(00)78903-9
Lee, P. H.; Kim, S.; Bull. Korean Chem. Soc. 1992, 13,580.
Kim, S.; Park, J. H.; Kim, Y. G.; Lee, J. M. J. Chem. Soc.,Chem. Commun. 1993, 1188.
Kim, S.; Lee, B. S.; Park, J. H.Bull. Korean Chem. Soc. 1993, 14, 654.
Lee, P. H.; Cho, M.; Han, I.-S.; Kim, S. Tetrahedron Lett. 1999,40, 6975. https://doi.org/10.1016/S0040-4039(99)01438-0
Jung, S. H.; Kim, J. H. Tetrahedron Lett., submitted.

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