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Competing pathways in the photo-Favorskii rearrangement and release of esters: Studies on fluorinated p-hydroxyphenacyl GABA and glutamate phototriggers
Three new trifluoromethylated p-hydroxyphenacyl (pHP) caged γ-aminobutyric acid (GABA) and glutamate (Glu) derivatives have been examined for their efficacy as photoremovable protecting groups in aqueous solution. By replacing hydrogen with fluorine, e.g., a m-trifluoromethyl or a m-trifluoromethoxy...
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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2009
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3422889/ https://ncbi.nlm.nih.gov/pubmed/19572582 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo900139h |
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