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Synthesis of new nucleoside analogs containing amino bisphosphonic groups

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Abstract

Adenosine derivatives containing a 2,2-bis(diethoxyphosphoryl)ethyl or 2,2-diphosphonoethyl group on the amino nitrogen atom were synthesized for the first time by reaction of 5′-chloro-5′-deoxy- and 5′-hydroxy-2′,3′-isopropylideneadenosine with tetraethyl ethene-1,1-diylbis(phosphonate) or tetrakis(trimethylsilyl) ethene-1,1-diylbis(phosphonate).

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Correspondence to L. I. Vagapova.

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Original Russian Text © L.I. Vagapova, A.V. Smolobochkin, A.S. Gazizov, A.R. Burilov, A.A. Bogdanov, M.A. Pudovik, O.G. Sinyashin, 2016, published in Zhurnal Organicheskoi Khimii, 2016, Vol. 52, No. 9, pp. 1347–1350.

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Vagapova, L.I., Smolobochkin, A.V., Gazizov, A.S. et al. Synthesis of new nucleoside analogs containing amino bisphosphonic groups. Russ J Org Chem 52, 1335–1338 (2016). https://doi.org/10.1134/S1070428016090141

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  • DOI: https://doi.org/10.1134/S1070428016090141

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