Phosphorylation of aminomethylated derivatives of 2,7-dihydroxynaphthalenes
- Authors: Slitikov P.V.1, Rasadkina E.N.2
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Affiliations:
- Bauman Moscow State Technical University
- Moscow State Pedagogical University
- Issue: Vol 86, No 3 (2016)
- Pages: 544-550
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/214180
- DOI: https://doi.org/10.1134/S1070363216030099
- ID: 214180
Cite item
Abstract
Phosphorylation of 2,7-dihydroxynaphthalene derivatives, containing different amine components was performed by full amides of phosphorous acid. A substantial effect of the intramolecular hydrogen bond on the process of phosphorylation was shown. Cyclophosphorylation was performed and principal possibility of the synthesis of naphthophosphacrownaphanes having aminomethyl linkers was shown. Mannich aminomethylation of naphthophosphacyclophanes was found to be impossible.
About the authors
P. V. Slitikov
Bauman Moscow State Technical University
Author for correspondence.
Email: pavlasiy@mail.ru
Russian Federation, ul. 2-ya Baumanskaya 5/1, Moscow, 105005
E. N. Rasadkina
Moscow State Pedagogical University
Email: pavlasiy@mail.ru
Russian Federation, Moscow
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