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Mendeleev Communications, 2010, Volume 20, Issue 1, Pages 4–6
DOI: https://doi.org/10.1016/j.mencom.2010.01.002
(Mi mendc2971)
 

This article is cited in 3 scientific papers (total in 3 papers)

Synthesis and structure of pyrimidinophanes with a sulfur atom in the spacer

A. E. Nikolaev, V. E. Semenov, O. A. Lodochnikova, Sh. K. Latypov, V. S. Reznik

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Abstract: The cyclization of 1,3-bis(ω-bromoalkyl)uracils with sodium sulfide led to pyrimidinophanes, containing one uracil unit and an S atom in the spacer, macrocyclic structure was confirmed by X-ray data; the S atom in bridge can be oxidized into sulfoxide or sulfone or converted into sulfonium ion.
Keywords: macrocycle, pyrimidinophane, uracil, cyclization, sulfonium salts.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (144.4 Kb)


Citation: A. E. Nikolaev, V. E. Semenov, O. A. Lodochnikova, Sh. K. Latypov, V. S. Reznik, “Synthesis and structure of pyrimidinophanes with a sulfur atom in the spacer”, Mendeleev Commun., 20:1 (2010), 4–6
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  • This publication is cited in the following 3 articles:
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