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Ferrocenoyl-adenines: substituent effects on regioselective acylation
A series of N(6)-substituted adenine–ferrocene conjugates was prepared and the reaction mechanism underlying the synthesis was explored. The S(N)2-like reaction between ferrocenoyl chloride and adenine anions is a regioselective process in which the product ratio (N7/N9-ferrocenoyl isomers) is gover...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520867/ https://www.ncbi.nlm.nih.gov/pubmed/36225728 http://dx.doi.org/10.3762/bjoc.18.133 |