Alkyl, unsaturated, (hetero)aryl, and N-protected α-amino ketones by acylation of organometallic reagents

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Abstract

Stable and easily accessible N-acylbenzotriazoles, derived from a variety of aliphatic, unsaturated, (hetero)aromatic, and N-protected α-amino carboxylic acids, were reacted with Grignard and heteroaryllithium reagents to afford corresponding ketones in good to excellent yields. © 2006 American Chemical Society.

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Katritzky, A. R., Le, K. N. B., Khelashvili, L., & Mohapatra, P. P. (2006). Alkyl, unsaturated, (hetero)aryl, and N-protected α-amino ketones by acylation of organometallic reagents. Journal of Organic Chemistry, 71(26), 9861–9864. https://doi.org/10.1021/jo0614801

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