2,5-Dimethylphenacyl as a new photoreleasable protecting group for carboxylic acids
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
10841481
DOI
10.1021/ol005789x
PII: ol005789x
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
The 2,5-dimethylphenacyl chromophore, a new photoremovable protecting group for carboxylic acids, is proposed. Direct photolysis of various 2,5-dimethylphenacyl esters in benzene or methanol at 254-366 nm leads to the formation of the corresponding carboxylic acids in almost quantitative isolated yields. The photodeprotection is based on efficient intramolecular hydrogen abstraction without the necessity of introducing a photosensitizer.
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