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Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone

Anna Evgen'evna Ivanova 1
Anna Evgen'evna Ivanova
Yanina Valer'evna Burgart 1
Yanina Valer'evna Burgart
Viktor Ivanovich Saloutin 1
Viktor Ivanovich Saloutin
Published 2016-03-02
CommunicationVolume 26, Issue 2, 106-108
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Ivanova A. E., Burgart Y. V., Saloutin V. I. Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone // Mendeleev Communications. 2016. Vol. 26. No. 2. pp. 106-108.
GOST all authors (up to 50) Copy
Ivanova A. E., Burgart Y. V., Saloutin V. I. Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone // Mendeleev Communications. 2016. Vol. 26. No. 2. pp. 106-108.
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TY - JOUR
DO - 10.1016/j.mencom.2016.03.006
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.006
TI - Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone
T2 - Mendeleev Communications
AU - Ivanova, Anna Evgen'evna
AU - Burgart, Yanina Valer'evna
AU - Saloutin, Viktor Ivanovich
PY - 2016
DA - 2016/03/02
PB - Mendeleev Communications
SP - 106-108
IS - 2
VL - 26
ER -
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@article{2016_Ivanova,
author = {Anna Evgen'evna Ivanova and Yanina Valer'evna Burgart and Viktor Ivanovich Saloutin},
title = {Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.006},
number = {2},
pages = {106--108},
doi = {10.1016/j.mencom.2016.03.006}
}
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Ivanova, Anna Evgen'evna, et al. “Non-natural nucleosides bearing 4-aryldiazenylpyrazole aglycone.” Mendeleev Communications, vol. 26, no. 2, Mar. 2016, pp. 106-108. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.03.006.

Abstract

Ribosylation of 4-aryldiazenyl-3-R-5-R-pyrazoles with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose in the presence of tin(IV) chloride gives α- and β-anomeric N-(2,3,5-tri-O-acetylribofuranosyl)-substituted derivatives. Their HPLC separation and deacetylation (MeOH, MeONa) affords 1-(β-D-ribofuranosyl)-3-R-5-R-4-(aryldiazenyl)-1H-pyrazoles.

References

1.
New Trends in Synthesis of Pyrazole Nucleosides as New Antimetabolites
Elgemeie G.H., Zaghary W.A., Amin K.M., Nasr T.M.
Nucleosides, Nucleotides and Nucleic Acids, 2005
2.
Design, synthesis and antiproliferative activity of methyl 4-Iodo-1-β-D-ribofuranosyl-pyrazole-3-carboxylate and related compounds
Manfredini S., Bazzanini R., Baraldi P.G., Simoni D., Vertuani S., Pani A., Pinna E., Scintu F., Lichino D., Colla P.L.
Bioorganic and Medicinal Chemistry Letters, 1996
4.
The Synthesis and Antiviral Activity of 4-Fluoro-1-β-D-ribofuranosyl-1H-pyrazole-3-carboxamide
Storer R., Ashton C.J., Baxter A.D., Hann M.M., Marr C.L., Mason A.M., Mo C., Myers P.L., Noble S.A., Penn C.R., Weir N.G., Woods J.M., Coe P.L.
Nucleosides and Nucleotides, 1999
6.
Synthesis and Antibacterial Activity of N-Alkyl-Substituted 4-Aryldiazenylpyrazoles
Ivanova A.E., Burgart Y.V., Saloutin V.I.
Chemistry of Heterocyclic Compounds, 2013
7.
Synthesis and the reactions of trifluoromethylated 1,2,3-triketones 2-(het)arylhydrazones and 4,7-dihydroazolo[5,1-c]triazines
Khudina O.G., Shchegol’kov E.V., Burgart Y.V., Kodess M.I., Kazheva O.N., Chekhlov A.N., Shilov G.V., Dyachenko O.A., Saloutin V.I., Chupakhin O.N.
Journal of Fluorine Chemistry, 2005
9.
Geometric isomerism in the series of fluoroalkyl-containing 1,2,3-trione 2-arylhydrazones
Khudina O.G., Shchegol’kov E.V., Burgart Y.V., Kodess M.I., Saloutin V.I., Kazheva O.N., Shilov G.V., D’yachenko O.A., Grishina M.A., Potemkin V.A., Chupakhin O.N.
Russian Journal of Organic Chemistry, 2007
10.
10.1016/j.mencom.2016.03.006_bib0050
Sankpal
J. Chem. Pharm. Res., 2010
11.
A short history of SHELX
Sheldrick G.M.
Acta Crystallographica Section A Foundations of Crystallography, 2007