Photolysis of a phenacyl benzoate tethered with a phenol leads to a very efficient release of benzoic acid, which is suggested to occur by electron transfer and/or proton transfer from the remote phenol moiety to the triplet excited carbonyl. Photolysis of the compound in protic solvents forms a new keto[3,3]paracyclophane.
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| http://dx.doi.org/10.1039/d2ob00660j | DOI Listing |
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