Bis-, tris-, and tetrakis-N-(2-nitroxyethyl) derivatives of 1,1’-[methylenebis(oxy)]bis(triaz-1-ene 2-oxides)


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Synthesis of new potential NO donors in living organisms, 1,1’-[methylenebis(oxy)]bis(triaz- 1-ene 2-oxides) bearing from two to four 2-nitroxyethyl groups at the nitrogen atoms was accomplished. The developed synthetic approaches involves either nucleophilic substitution of the bromine atoms of the corresponding N-2-bromoethyl derivatives of 1,1’-[methylenebis(oxy)]-bis(triaz-1-ene 2-oxides) or nitration of its 2-hydroxyethyl analogs. Some of the synthesized compounds are of interest as promising energetic materials.

About the authors

G. A. Smirnov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Author for correspondence.
Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

P. B. Gordeev

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

S. V. Nikitin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

G. V. Pokhvisneva

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

T. V. Ternikova

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991

I. M. Chistokhvalov

D. Mendeleev University of Chemical Technology of Russia

Email: smir@ioc.ac.ru
Russian Federation, 9 Miusskaya pl., Moscow, 125047

O. A. Luk’yanov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: smir@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991


Copyright (c) 2018 Springer Science+Business Media, LLC, part of Springer Nature

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies