Oxidations by methyl (trifluoromethyl) dioxirane. 4.1 oxyfunctionalization of aromatic hydrocarbons
…, F Ciminale, M Fiorentino, C Fusco, T Prencipe…
Index: Mello, Rossella; Ciminale, Francesco; Fiorentino, Michele; Fusco, Caterina; Prencipe, Teresa; Curci, Ruggero Tetrahedron Letters, 1990 , vol. 31, # 42 p. 6097 - 6100
Full Text: HTML
Citation Number: 50
Abstract
Abstract By using the title dioxirane (1a), naphthalene (2), phenanthrene (3), and anthracene (4) have been converted into anti-naphthalene-1, 2; 3, 4-dioxide (2′), phenonthrene-9, 10-oxide (3′), and anthraquinone (4′), respectively, in high yield and under mild conditions. However, the transformation of pyrene (5)-an higher homologue of the polycyclic aromatic hydrocarbon series-into the corresponding arene oxide was found ...
Related Articles:
Direct epoxidation of polycyclic aromatic compounds by superoxide in the presence of phosgene dimer
[Nagano, Tetsuo; Yokoohji, Kiyomi; Hirobe, Masaaki Tetrahedron Letters, 1983 , vol. 24, # 33 p. 3481 - 3484]