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Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles

Zhanna Vyacheslavovna Chirkova 1
Zhanna Vyacheslavovna Chirkova
, 
Sergey Ivanovich Filimonov 1
Sergey Ivanovich Filimonov
, 
10.1016/j.mencom.2018.01.029
Published 2017-12-22
Communication , Volume 28, Issue 1, 86-87
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Chirkova Z. V., Filimonov S. I., Abramov I. G. Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 86-87.
GOST all authors (up to 50) Copy
Chirkova Z. V., Filimonov S. I., Abramov I. G. Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 86-87.
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TY - JOUR
DO - 10.1016/j.mencom.2018.01.029
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.029
TI - Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles
T2 - Mendeleev Communications
AU - Chirkova, Zhanna Vyacheslavovna
AU - Filimonov, Sergey Ivanovich
AU - Abramov, Igor Gennad'evich
PY - 2017
DA - 2017/12/22
PB - Mendeleev Communications
SP - 86-87
IS - 1
VL - 28
ER -
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@article{2017_Chirkova,
author = {Zhanna Vyacheslavovna Chirkova and Sergey Ivanovich Filimonov and Igor Gennad'evich Abramov},
title = {Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles},
journal = {Mendeleev Communications},
year = {2017},
volume = {28},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.029},
number = {1},
pages = {86--87},
doi = {10.1016/j.mencom.2018.01.029}
}
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Chirkova, Zhanna Vyacheslavovna, et al. “Synthesis of substituted [1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles.” Mendeleev Communications, vol. 28, no. 1, Dec. 2017, pp. 86-87. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.029.

Abstract

10-Aryl-2-oxo-2,3-dihydro-1H-[1,2,4]oxadiazino[2,3-a]indole-7,8-dicarbonitriles were obtained in two steps from the corresponding 2-amino-1-hydroxyindoles and methyl bromoacetate.

References

1.
Synthesis and reactivity of N-hydroxy-2-aminoindoles
Belley M., Sauer E., Beaudoin D., Duspara P., Trimble L.A., Dubé P.
Tetrahedron Letters, 2006
2.
Synthesis and Reactivity of N-Hydroxy-2-Amino-3-Arylindoles
Belley M., Beaudoin D., Duspara P., Sauer E., St-Pierre G., Trimble L.
Synlett, 2007
3.
Synthesis of 3-substituted 2-amino-1-hydroxy-1H-indole-5,6-dicarbonitriles
Filimonov S.I., Chirkova Z.V., Sharunov V.S., Abramov I.G., Stashina G.A., Firgang S.I., Suponitsky K.Y.
Chemistry of Heterocyclic Compounds, 2012
4.
Synthesis of 2-Aminoindole Derivatives with Hantzsch Ester Catalyzed by Pd/C
Xing R., Tian Q., Liu Q., Li Y.
Chinese Journal of Chemistry, 2012
5.
A Convenient Synthesis of 3,7′-Bisindole Derivatives
Liu T., Zhu H., Luo D., Yan S., Lin J.
Molecules, 2016
8.
Benzo[g]indoles
Pozharskii A.F., Kachalkina S.G., Gulevskaya A.V., Filatova E.A.
Russian Chemical Reviews, 2017
10.
An evaluation of synthetic indole derivatives as inhibitors of monoamine oxidase.
Chirkova Z.V., Kabanova M.V., Filimonov S.I., Abramov I.G., Petzer A., Petzer J.P., Suponitsky K.Y.
Bioorganic and Medicinal Chemistry Letters, 2016
11.
Synthesis and antimicrobial activity of certain 6H-1,2,4-oxadiazin-3(2H)-ones
Berkowitz P.T., Long R.A., Dea P., Robins R.K., Matthews T.R.
Journal of Medicinal Chemistry, 1977
12.
Synthesis of N-Alkyl-1,2,4-oxadiazinones as Angiotensin-II (AT1) Receptor Antagonists
N. Weller H., V. Miller A., E. J. Dickinson K., Anders Hedberg S., L. Delaney C., P. Serafino R., Moreland S.
Heterocycles, 1993
13.
Novel resolution of chiral lactams
Ürögdi L., Kisfaludy L., Patthy Á., Vezér C.
Journal of Heterocyclic Chemistry, 1989
16.
Facile access to novel 1,2,4-oxadiazinan-5-ones via [3 + 3] cycloaddition of in situ generated azaoxyallyl cations with nitrones
Zhao H., Zhao Y., Liu Y., Zhao L., Feng N., Pang H., Chen X., Song X., Du J.
RSC Advances, 2017
18.
Synthesis of N-substituted 1-hydroxypyrrolo[3,4-f]indol-5,7-diones
Chirkova Z.V., Kabanova M.V., Filimonov S.I., Sergeev S.S., Smirnova E.A., Sudzilovskaya T.N.
Russian Journal of Organic Chemistry, 2017
20.
Regioselective Fischer indole route to 3-unsubstituted indoles
Zhao D., Hughes D.L., Bender D.R., DeMarco A.M., Reider P.J.
Journal of Organic Chemistry, 1991