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Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines

Maxim Anatolyevich Mironov 1
Maxim Anatolyevich Mironov
, 
Vladimir Stepanovich Mokrushin 1
Vladimir Stepanovich Mokrushin
10.1070/MC1998v008n06ABEH001017
Published 1998-12-16
Communication , Volume 8, Issue 6, 242-243
11
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Mironov M. A., Mokrushin V. S. Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 242-243.
GOST all authors (up to 50) Copy
Mironov M. A., Mokrushin V. S. Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 242-243.
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TY - JOUR
DO - 10.1070/MC1998v008n06ABEH001017
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001017
TI - Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines
T2 - Mendeleev Communications
AU - Mironov, Maxim Anatolyevich
AU - Mokrushin, Vladimir Stepanovich
PY - 1998
DA - 1998/12/16
PB - Mendeleev Communications
SP - 242-243
IS - 6
VL - 8
ER -
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@article{1998_Mironov,
author = {Maxim Anatolyevich Mironov and Vladimir Stepanovich Mokrushin},
title = {Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001017},
number = {6},
pages = {242--243},
doi = {10.1070/MC1998v008n06ABEH001017}
}
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Mironov, Maxim Anatolyevich, and Vladimir Stepanovich Mokrushin. “Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines.” Mendeleev Communications, vol. 8, no. 6, Dec. 1998, pp. 242-243. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001017.

Abstract

A new reaction between aromatic isocyanides containing electron-withdrawing substituents and triethylamine is described which allows 2-triethylammonium-3-arylaminoindolates to be obtained. The structure of the compounds was determined by X-ray analysis, NMR and mass spectroscopy

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