Intramolecular proton transfer in photohydration reactions

P Kalanderopoulos, K Yates

Index: Kalanderopoulos, Peter; Yates, Keith Journal of the American Chemical Society, 1986 , vol. 108, # 20 p. 6290 - 6295

Full Text: HTML

Citation Number: 37

Abstract

Abstract: The photohydration by intramolecular proton transfer of compounds 1-12 has been studied. The non-nitro-substituted o-hydroxystyrenes photohydrate cleanly via the Markovnikov addition of water to afford the 1-arylethanols. The nitro-substituted o- hydroxystyrenes showed no dependence of product quantum yield with change in pH. The products isolated and identified in this case were the corresponding 2-(2-hydroxyphenyl) ...

Related Articles:

Alkylation of dianions derived from 2-(1-iminoalkyl) phenols: synthesis of functionalized 2-acyl phenols

[Cimarelli, Cristina; Palmieri, Gianni Tetrahedron, 1998 , vol. 54, # 51 p. 15711 - 15720]

Regioselective reductive openings of acetals; mechanistic details and synthesis of fluorescently labeled compounds

[Johnsson, Richard; Mani, Katrin; Cheng, Fang; Ellervik, Ulf Journal of Organic Chemistry, 2006 , vol. 71, # 9 p. 3444 - 3451]

More Articles...