3849-34-1Relevant articles and documents
Pryor,Kaplan
, p. 4234,4235, 4236 (1964)
PHOTOCHEMICAL REACTION OF ALCOHOLS - II. IRRADIATION OF AROMATIC ALCOHOLS
Balsells, R. Erra,Frasca, A. R.
, p. 2525 - 2538 (2007/10/02)
The UV irradiation of aromatic alcohols leads to the formation of several products: carbonyl compounds, ethers, α-glycols and tetra-aryl-1,4-dioxanes.The photoformation of α-glycols is qualitatively and quantitatively compared to the photoreduction of the carbonyl compounds.It is noteworthy that the glycols are formed with a stereochemistry very different depending upon whether the substrate is an alcohol or a carbonyl compound.The structure, configuration and conformation of the 1,4-dioxanes obtained are studied as well as their origin.Other aspects of the photochemistry of the alcohols are analyzed using hydroperoxides as model substrates.