This article is cited in 10 scientific papers (total in 10 papers)
New Macrocyclic Systems – Tetrafurazano[3,4-c:3,4-e:3,4-i:3,4-k]-1,2,7,8-tetraazacyclododeca-1,3,5,7,9,11-hexane and Hexafurazano-[3,4-c:3,4-e:3,4-i:3,4-k:3,4-o:3,4-r]-1,2,7,8,13,14-hexaazacyclooctadeca-1,3,5,7,9,11,13,15,17-nonane by Oxidative Macrocyclization of Diaminodifurazanyl
Abstract:
The title compounds have been synthesised by interaction of diaminodifurazanyl with dibromoisocyanurate (DBI) and it was shown that the diazene fragment in such structures is capable of being oxidized into a diazene oxide fragment.
Document Type:
Article
Language: English
Citation:
M. A. Epishina, N. N. Makhova, L. V. Batog, L. S. Konstantinova, L. I. Khmel'nitskii, “New Macrocyclic Systems – Tetrafurazano[3,4-c:3,4-e:3,4-i:3,4-k]-1,2,7,8-tetraazacyclododeca-1,3,5,7,9,11-hexane and Hexafurazano-[3,4-c:3,4-e:3,4-i:3,4-k:3,4-o:3,4-r]-1,2,7,8,13,14-hexaazacyclooctadeca-1,3,5,7,9,11,13,15,17-nonane by Oxidative Macrocyclization of Diaminodifurazanyl”, Mendeleev Commun., 4:3 (1994), 102
Linking options:
https://www.mathnet.ru/eng/mendc5173
https://www.mathnet.ru/eng/mendc/v4/i3/p102
This publication is cited in the following 10 articles:
V. Yu. Rozhkov, L. V. Batog, M. I. Struchkova, “Nucleophilic substitution in the series of (1,2,3-triazol-1-yl)-1,2,5-oxadiazoles. Reactions with N-, O-, and S-nucleophiles”, Russ Chem Bull, 54:8 (2005), 1923
Aleksei B. Sheremetev, Nataliya S. Aleksandrova, Dmitrii E. Dmitriev, Boris B. Averkiev, Mikhail Yu. Antipin, “Synthesis and x-ray study of novel azofurazan-annulated macrocyclic lactams”, Journal of Heterocyclic Chemistry, 42:4 (2005), 519
Aleksei B. Sheremetev, Elena V. Shatunova, Boris B. Averkiev, Dmitrii E. Dmitriev, Viktor A. Petukhov, Mikhail Yu. Antipin, “Chromophoric macrocycles from the oxidation of bis(aminofurazanylic) ethers of 1,2‐diols”, Heteroatom Chemistry, 15:2 (2004), 131
Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65
A. N. Blinnikov, N. N. Makhova, L. I. Khmel'nitskii, “New approaches to the preparation of azoxyfuroxans”, Mendeleev Commun., 9:1 (1999), 15–17
V. A. Eman, M. S. Sukhanov, O. V. Lebedev, L. V. Batog, L. S. Konstantinova, V. Yu. Rozhkov, M. O. Dekaprilevich, Yu. T. Struchkov, L. I. Khmel'nitskii, “First representatives of macrocyclic poly(diazene oxide furazans): 3,4:7,8:11,12:15,16-tetrafurazano-1,2,5,6,9,10,13,14-octaazacyclohexadeca-1,3,5,7,9,11,13,15-octaene 1,9- and 1,10-dioxides; 1,5,9,13-tetraoxide and its crystal structure”, Mendeleev Commun., 7:1 (1997), 5–7
Comprehensive Heterocyclic Chemistry II, 1996, 905
R. Michael Paton, Comprehensive Heterocyclic Chemistry II, 1996, 229
L. V. Batog, V. Yu. Rozhkov, L. S. Konstantinova, V. E. Eman, M. O. Dekaprilevich, Yu. T. Struchkov, S. E. Semenov, O. V. Lebedev, L. I. Khmel'nitskii, “Oxidative macrocyclocondensation of 3,4-diaminofurazan and 4,4?-diamino-3,3?-azofurazan with dibromoisocyanurate. Crystal structures of hexa- and octadiazenofurazan macrocycles”, Russ Chem Bull, 45:5 (1996), 1189
Peter J. Steel, Advances in Heterocyclic Chemistry, 67, 1996, 1