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Stereoselective Synthesis of 24-Fluoro-25-Hydroxyvitamin D(3) Analogues and Their Stability to hCYP24A1-Dependent Catabolism
Two 24-fluoro-25-hydroxyvitamin D(3) analogues (3,4) were synthesized in a convergent manner. The introduction of a stereocenter to the vitamin D(3) side-chain C24 position was achieved via Sharpless dihydroxylation, and a deoxyfluorination reaction was utilized for the fluorination step. Comparison...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584271/ https://www.ncbi.nlm.nih.gov/pubmed/34769295 http://dx.doi.org/10.3390/ijms222111863 |