Direct Photolysis of Phenacyl Protecting Groups Studied by Laser Flash Photolysis: An Excited State Hydrogen Atom Abstraction Pathway Leads to Formation of Carboxylic Acids and Acetophenone
- 17 March 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (12) , 2965-2966
- https://doi.org/10.1021/ja971431t
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Photochemistry of Arylmethyl Esters in Nucleophilic Solvents: Radical Pair and Ion Pair IntermediatesAccounts of Chemical Research, 1997
- Photochemistry of phosphate esters: .alpha.-keto phosphates as a photoprotecting group for caged phosphateJournal of the American Chemical Society, 1993
- Synthetic, mechanistic and photochemical studies of phosphate esters of substituted benzoinsJournal of the Chemical Society, Perkin Transactions 1, 1992
- Control of product distribution by Marcus type electron-transfer rates for the radical pair generated in benzylic ester photochemistryJournal of the American Chemical Society, 1989
- Study of the long-lived intermediate formed in the photoreduction of benzophenone by isopropyl alcoholJournal of Photochemistry and Photobiology A: Chemistry, 1989
- p-Methoxyphenacyl esters as photodeblockable protecting groups for phosphatesJournal of the Chemical Society, Chemical Communications, 1987
- Direct Observation of Acetophenone Enol Formed by Photohydration of PhenylacetyleneHelvetica Chimica Acta, 1986
- Acidity of Acetophenone Enol in Aqueous SolutionAngewandte Chemie International Edition in English, 1979
- Photolysis of Desyl Compounds. A New Photolytic CyclizationJournal of the American Chemical Society, 1964
- Photochemical Reactions of Benzophenone in Alcohols1Journal of the American Chemical Society, 1959