Home / Publications / Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan

Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan

Alexey Mikhailovich Starosotnikov 1
Alexey Mikhailovich Starosotnikov
, 
Maxim Aleksandrovich Bastrakov 1
Maxim Aleksandrovich Bastrakov
, 
Alexander Alexandrovich Pavlov 2
Alexander Alexandrovich Pavlov
,  , 
Igor L'vovich Dalinger 1
Igor L'vovich Dalinger
, 
Svyatoslav Arkad'evich Shevelev 1
Svyatoslav Arkad'evich Shevelev
10.1016/j.mencom.2016.04.013
Published 2016-04-28
Communication , Volume 26, Issue 3, 217-219
23
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Starosotnikov A. M. et al. Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan // Mendeleev Communications. 2016. Vol. 26. No. 3. pp. 217-219.
GOST all authors (up to 50) Copy
Starosotnikov A. M., Bastrakov M. A., Pavlov A. A., Fedyanin I. V., Dalinger I. L., Shevelev S. A. Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan // Mendeleev Communications. 2016. Vol. 26. No. 3. pp. 217-219.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2016.04.013
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.04.013
TI - Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan
T2 - Mendeleev Communications
AU - Starosotnikov, Alexey Mikhailovich
AU - Bastrakov, Maxim Aleksandrovich
AU - Pavlov, Alexander Alexandrovich
AU - Fedyanin, Ivan Vladimirovich
AU - Dalinger, Igor L'vovich
AU - Shevelev, Svyatoslav Arkad'evich
PY - 2016
DA - 2016/04/28
PB - Mendeleev Communications
SP - 217-219
IS - 3
VL - 26
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2016_Starosotnikov,
author = {Alexey Mikhailovich Starosotnikov and Maxim Aleksandrovich Bastrakov and Alexander Alexandrovich Pavlov and Ivan Vladimirovich Fedyanin and Igor L'vovich Dalinger and Svyatoslav Arkad'evich Shevelev},
title = {Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.04.013},
number = {3},
pages = {217--219},
doi = {10.1016/j.mencom.2016.04.013}
}
MLA
Cite this
MLA Copy
Starosotnikov, Alexey Mikhailovich, et al. “Synthesis of novel polycyclic heterosystems based on 5-nitro[1,2,5]thiadiazolo[3,4-e]benzofuroxan.” Mendeleev Communications, vol. 26, no. 3, Apr. 2016, pp. 217-219. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.04.013.

Abstract

The Diels–Alder and Michael reactions of 5-nitro[1,2,5]-thiadiazolo[3,4-e]benzofuroxan afforded complex polycyclic compounds with potential NO-donor activity containing furoxan moiety along with another heterocyclic pharmacophoric fragments.

References

1.
Ananikov V.P., Khokhlova E.A., Egorov M.P., Sakharov A.M., Zlotin S.G., Kucherov A.V., Kustov L.M., Gening M.L., Nifantiev N.E.
Mendeleev Communications, 2015
2.
Zlotin S.G., Churakov A.M., Luk’yanov O.A., Makhova N.N., Sukhorukov A.Y., Tartakovsky V.A.
Mendeleev Communications, 2015
3.
Facile Dearomatization of Nitroquinolines through [3+2] and [4+2] Cycloaddition Reactions
Bastrakov M.A., Starosotnikov A.M., Kachala V.V., Fedyanin I.V., Shevelev S.A.
Asian Journal of Organic Chemistry, 2015
4.
Bastrakov M.A., Starosotnikov A.M., Fedyanin I.V., Kachala V.V., Shevelev S.A.
Mendeleev Communications, 2014
5.
3-R-4-Nitro-6,7-furoxanobenzo[d]isoxazoles – a new type of condensed nitroarenes capable of Diels–Alder reaction
Bastrakov M.A., Starosotnikov A.M., Kachala V.V., Dalinger I.L., Shevelev S.A.
Chemistry of Heterocyclic Compounds, 2015
6.
Pharmacological Properties of Furoxans and Benzofuroxans: Recent Developments
Cerecetto H., Porcal W.
Mini-Reviews in Medicinal Chemistry, 2005
7.
Benzofuroxan and Furoxan. Chemistry and Biology
Cerecetto H., González M.
Topics in Heterocyclic Chemistry, 2007
9.
Korolev S.P., Kondrashina O.V., Druzhilovsky D.S., Starosotnikov A.M., Dutov M.D., Bastrakov M.A., Dalinger I.L., Filimonov D.A., Shevelev S.A., Poroikov V.V., Agapkina Y.Y., Gottikh M.B.
Acta Naturae, 2013
10.
Exogenous nitric oxide donors and inhibitors of its formation (the chemical aspects)
Granik V.G., Ryabova S.Y., Grigoriev N.B.
Russian Chemical Reviews, 1997
12.
Heterocyclic NO prodrugs
Schönafinger K.
Il Farmaco, 1999
13.
Thiol-mediated generation of nitric oxide accounts for the vasodilator action of furoxans
Feelisch M., Schönafingeri K., Noack H.
Biochemical Pharmacology, 1992
14.
Furoxans as Nitric Oxide Donors. 4-Phenyl-3-furoxancarbonitrile: Thiol-Mediated Nitric Oxide Release and Biological Evaluation
Medana C., Ermondi G., Fruttero R., Di Stilo A., Ferretti C., Gasco A.
Journal of Medicinal Chemistry, 1994
15.
Fershtat L.L., Epishina M.A., Kulikov A.S., Makhova N.N.
Mendeleev Communications, 2015
18.
Synthesis and Anti-HIV Activity of 4-(Naphthalen-1-yl)-1,2,5-thiadiazol-3-hydroxyl Derivatives
Rai D., Chen W., Zhan P., Liu H., Tian Y., Liang X., De Clercq E., Pannecouque C., Balzarini J., Liu X.
Chemical Biology and Drug Design, 2014
19.
Antitumor Activity of Some Novel 1,2,5-Thiadiazole Derivatives
Ismail Z.H., Ghorab M.M., Mohamed E.M., Aly H.M., El-Gaby M.S.
Phosphorus, Sulfur and Silicon and the Related Elements, 2008
20.
Muscarinic agonists as analgesics. Antinociceptive activity versus M1 activity: SAR of alkylthio-TZTP's and related 1,2,5-thiadiazole analogs.
Sauerberg P., Olesen P.H., Sheardown M.J., Suzdak P.D., Shannon H.E., Bymaster F.P., Calligaro D.O., Mitch C.H., Ward J.S., Swedberg M.D.
Life Sciences, 1995
21.
Muscarinic Agonists with Antipsychotic-like Activity:  Structure−Activity Relationships of 1,2,5-Thiadiazole Analogues with Functional Dopamine Antagonist Activity
Sauerberg P., Jeppesen L., Olesen P.H., Rasmussen T., Swedberg M.D., Sheardown M.J., Fink-Jensen A., Thomsen C., Thøgersen H., Rimvall K., Ward J.S., Calligaro D.O., DeLapp N.W., Bymaster F.P., Shannon H.E., et. al.
Journal of Medicinal Chemistry, 1998
22.
10.1016/j.mencom.2016.04.013_bib0065
Pesin
Zh. Obshch. Khim., 1964
23.
The nitroolefinic behavior of 4-nitrobenzodifuroxan
Kurbatov S., Goumont R., Marrot J., Terrier F.
Tetrahedron Letters, 2004
24.
Superelectrophilicity of the Nitroolefinic Fragment of 4-Nitrobenzodifuroxan in Michael-Type Reactions with Indoles: A Kinetic Study in Acetonitrile
Lakhdar S., Goumont R., Berionni G., Boubaker T., Kurbatov S., Terrier F.
Chemistry - A European Journal, 2007
25.
Crystal structure refinement withSHELXL
Sheldrick G.M.
Acta crystallographica. Section C, Structural chemistry, 2015