Reinvestigation of the synthetic and mechanistic aspects of Mn(III) acetate mediated oxidation of enones

2004-04-05
Demir, Ayhan Sıtkı
Reis, O
Igdir, AC
Mn(OAc)(3) mediated alpha'-acetoxylation of alpha,beta-unsaturated enones is reinvestigated from a synthetic and mechanistic point of view and an improved procedure based on the use of acetic acid as a co-solvent is presented. Excellent results were obtained for a variety of structurally diverse and synthetically important enones under the optimized conditions.
Citation Formats
A. S. Demir, O. Reis, and A. Igdir, “Reinvestigation of the synthetic and mechanistic aspects of Mn(III) acetate mediated oxidation of enones,” TETRAHEDRON, vol. 60, no. 15, pp. 3427–3432, 2004, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/56762.