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On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH

[Image: see text] Jakeman et al. recently reported the inability to distinguish the diastereomers of uridine 5′-β,γ-fluoromethylenetriphosphate (β,γ-CHF-UTP, 1) by (19)F NMR under conditions we previously prescribed for the resolution of the corresponding β,γ-CHF-dGTP spectra, stating further that 1...

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Autores principales: Hwang, Candy S., Kashemirov, Boris A., McKenna, Charles E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059216/
https://www.ncbi.nlm.nih.gov/pubmed/24819695
http://dx.doi.org/10.1021/jo500452b
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author Hwang, Candy S.
Kashemirov, Boris A.
McKenna, Charles E.
author_facet Hwang, Candy S.
Kashemirov, Boris A.
McKenna, Charles E.
author_sort Hwang, Candy S.
collection PubMed
description [Image: see text] Jakeman et al. recently reported the inability to distinguish the diastereomers of uridine 5′-β,γ-fluoromethylenetriphosphate (β,γ-CHF-UTP, 1) by (19)F NMR under conditions we previously prescribed for the resolution of the corresponding β,γ-CHF-dGTP spectra, stating further that 1 decomposed under these basic conditions. Here we show that the (19)F NMR spectra of 1 (∼1:1 diastereomer mixture prepared by coupling of UMP-morpholidate with fluoromethylenebis(phosphonic acid)) in D(2)O at pH 10 are indeed readily distinguishable. 1 in this solution was stable for 24 h at rt.
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spelling pubmed-40592162015-05-12 On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH Hwang, Candy S. Kashemirov, Boris A. McKenna, Charles E. J Org Chem [Image: see text] Jakeman et al. recently reported the inability to distinguish the diastereomers of uridine 5′-β,γ-fluoromethylenetriphosphate (β,γ-CHF-UTP, 1) by (19)F NMR under conditions we previously prescribed for the resolution of the corresponding β,γ-CHF-dGTP spectra, stating further that 1 decomposed under these basic conditions. Here we show that the (19)F NMR spectra of 1 (∼1:1 diastereomer mixture prepared by coupling of UMP-morpholidate with fluoromethylenebis(phosphonic acid)) in D(2)O at pH 10 are indeed readily distinguishable. 1 in this solution was stable for 24 h at rt. American Chemical Society 2014-05-12 2014-06-06 /pmc/articles/PMC4059216/ /pubmed/24819695 http://dx.doi.org/10.1021/jo500452b Text en Copyright © 2014 American Chemical Society
spellingShingle Hwang, Candy S.
Kashemirov, Boris A.
McKenna, Charles E.
On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title_full On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title_fullStr On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title_full_unstemmed On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title_short On the Observation of Discrete Fluorine NMR Spectra for Uridine 5′-β,γ-Fluoromethylenetriphosphate Diastereomers at Basic pH
title_sort on the observation of discrete fluorine nmr spectra for uridine 5′-β,γ-fluoromethylenetriphosphate diastereomers at basic ph
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059216/
https://www.ncbi.nlm.nih.gov/pubmed/24819695
http://dx.doi.org/10.1021/jo500452b
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