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Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles

Zhanna Vyacheslavovna Chirkova
Mariya Valer'evna Kabanova 1
Mariya Valer'evna Kabanova
Sergey S Sergeev 1
Sergey S Sergeev
Sergey Ivanovich Filimonov 1
Sergey Ivanovich Filimonov
Alexander Viktorovich Samet 2
Alexander Viktorovich Samet
Kirill Yu Suponitsky 3
Kirill Yu Suponitsky
Published 2015-07-08
CommunicationVolume 25, Issue 4, 315-317
15
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Chirkova Z. V. et al. Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 315-317.
GOST all authors (up to 50) Copy
Chirkova Z. V., Kabanova M. V., Sergeev S. S., Filimonov S. I., Abramov I. G., Samet A. V., Suponitsky K. Yu. Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 315-317.
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TY - JOUR
DO - 10.1016/j.mencom.2015.07.030
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.030
TI - Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles
T2 - Mendeleev Communications
AU - Chirkova, Zhanna Vyacheslavovna
AU - Kabanova, Mariya Valer'evna
AU - Sergeev, Sergey S
AU - Filimonov, Sergey Ivanovich
AU - Abramov, Igor Gennad'evich
AU - Samet, Alexander Viktorovich
AU - Suponitsky, Kirill Yu
PY - 2015
DA - 2015/07/08
PB - Mendeleev Communications
SP - 315-317
IS - 4
VL - 25
ER -
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@article{2015_Chirkova,
author = {Zhanna Vyacheslavovna Chirkova and Mariya Valer'evna Kabanova and Sergey S Sergeev and Sergey Ivanovich Filimonov and Igor Gennad'evich Abramov and Alexander Viktorovich Samet and Kirill Yu Suponitsky},
title = {Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.030},
number = {4},
pages = {315--317},
doi = {10.1016/j.mencom.2015.07.030}
}
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Chirkova, Zhanna Vyacheslavovna, et al. “Synthesis of 3-acyl-1-hydroxy-1H-indole-5,6-dicarbonitriles.” Mendeleev Communications, vol. 25, no. 4, Jul. 2015, pp. 315-317. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.030.

Abstract

The Vilsmeier–Haack formylation of 4-(2-aryl-2-oxoethyl)-5-nitrophthalonitriles followed by reduction affords 3-acyl-1-hydroxy- 1H-indole-5,6-dicarbonitriles.

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