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Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines

Maxim Anatolyevich Mironov 1
Maxim Anatolyevich Mironov
, 
Maria Igorevna Tokareva 1
Maria Igorevna Tokareva
, 
Vladimir Stepanovich Mokrushin 1
Vladimir Stepanovich Mokrushin
10.1016/j.mencom.2007.11.020
Published 2007-11-09
Communication , Volume 17, Issue 6, 354-356
4
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Mironov M. A., Tokareva M. I., Mokrushin V. S. Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines // Mendeleev Communications. 2007. Vol. 17. No. 6. pp. 354-356.
GOST all authors (up to 50) Copy
Mironov M. A., Tokareva M. I., Mokrushin V. S. Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines // Mendeleev Communications. 2007. Vol. 17. No. 6. pp. 354-356.
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TY - JOUR
DO - 10.1016/j.mencom.2007.11.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.11.020
TI - Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines
T2 - Mendeleev Communications
AU - Mironov, Maxim Anatolyevich
AU - Tokareva, Maria Igorevna
AU - Mokrushin, Vladimir Stepanovich
PY - 2007
DA - 2007/11/09
PB - Mendeleev Communications
SP - 354-356
IS - 6
VL - 17
ER -
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@article{2007_Mironov,
author = {Maxim Anatolyevich Mironov and Maria Igorevna Tokareva and Vladimir Stepanovich Mokrushin},
title = {Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines},
journal = {Mendeleev Communications},
year = {2007},
volume = {17},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.11.020},
number = {6},
pages = {354--356},
doi = {10.1016/j.mencom.2007.11.020}
}
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Mironov, Maxim Anatolyevich, et al. “Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines.” Mendeleev Communications, vol. 17, no. 6, Nov. 2007, pp. 354-356. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.11.020.

Keywords

indoles
isocyanides
reaction design

Abstract

The reaction of N,N-dialkylbenzylamines with aromatic isocyanides leading to 2-dialkylamino-3-aryliminoindole derivatives with the subsequent formation of zwitter ionic indolates has been discovered; the structures of final products have been confirmed by X-ray analysis.

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