Phenolic oxidation with (diacetoxyiodo) benzene
A Pelter, S Elgendy
Index: Pelter, Andrew; Elgendy, Said Tetrahedron Letters, 1988 , vol. 29, # 6 p. 677 - 680
Full Text: HTML
Citation Number: 163
Abstract
(Diacetoxyiodo)benzene oxidises quinols and extended quinols to the corresponding quinones smoothly and in high yield. Excess of the reagent in methanol with monohydric phenols directly yields -quinone ketals, also in good yields. 4-Alkyl and 4-alkoxyphenols give the corresponding 4-alkyl-4-methoxycyclohexadienones and 4-alkoxy-4-methoxycyclohexadienones. ... (Diacetoxyiodo)benzene in methanol smoothly oxidises phenols in excellent yields.
Related Articles:
[Dohi, Toshifumi; Kamitanaka, Tohru; Watanabe, Shohei; Hu, Yinjun; Washimi, Naohiko; Kita, Yasuyuki Chemistry - A European Journal, 2012 , vol. 18, # 43 p. 13614 - 13618]
[Hu, Yinjun; Kamitanaka, Tohru; Mishima, Yusuke; Dohi, Toshifumi; Kita, Yasuyuki Journal of Organic Chemistry, 2013 , vol. 78, # 11 p. 5530 - 5543]