Palladium-catalyzed addition of hydroxylamine derivatives to Baylis-Hillman acetate adducts

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Abstract

The first use of hydroxylamine derivatives as the aminoxy equivalent of nucleophiles in palladium catalyzed addition to Baylis-Hillman acetate adducts is described. The reaction proceeds smoothly to give the substituted allyloxy amines in good yield and selectivity. © 2006 Elsevier Ltd. All rights reserved.

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Raji Reddy, C., Kiranmai, N., Kiran Babu, G. S., Dattatreya Sarma, G., Jagadeesh, B., & Chandrasekhar, S. (2007). Palladium-catalyzed addition of hydroxylamine derivatives to Baylis-Hillman acetate adducts. Tetrahedron Letters, 48(2), 215–218. https://doi.org/10.1016/j.tetlet.2006.11.061

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