Reinvestigation of the synthetic and mechanistic aspects of Mn (III) acetate mediated oxidation of enones
AS Demir, Ö Reis, AC Igdir
Index: Demir, Ayhan S.; Reis, Oemer; Igdir, A. Cigdem Tetrahedron, 2004 , vol. 60, # 15 p. 3427 - 3432
Full Text: HTML
Citation Number: 34
Abstract
Mn (OAc) 3 mediated α′-acetoxylation of α, β-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.
Related Articles:
[Demir, Ayhan S.; Findik, Hamide Tetrahedron, 2008 , vol. 64, # 27 p. 6196 - 6201]
[Tamura, Yasumitsu; Yakura, Takayuki; Terashi, Hiroaki; Haruta, Jun-Ichi; Kita, Yasuyuki Chemical & Pharmaceutical Bulletin, 1987 , vol. 35, # 2 p. 570 - 577]
[House,H.O. et al. Journal of the American Chemical Society, 1970 , vol. 92, p. 2800 - 2810]
[Tamura, Yasumitsu; Yakura, Takayuki; Terashi, Hiroaki; Haruta, Jun-Ichi; Kita, Yasuyuki Chemical & Pharmaceutical Bulletin, 1987 , vol. 35, # 2 p. 570 - 577]
[Rubottom,G.M.; Gruber,J.M. Journal of Organic Chemistry, 1978 , vol. 43, # 8 p. 1599 - 1602]