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Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene

Alexander Yur'evich Rulev 1
Alexander Yur'evich Rulev
, 
Alexander Sergeevich Mokov 1
Alexander Sergeevich Mokov
, 
Mikhail Grigor'evich Voronkov 1
Mikhail Grigor'evich Voronkov
10.1070/MC1995v005n02ABEH000454
Published 1995-04-30
Communication , Volume 5, Issue 2, 53-55
5
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Rulev A. Y., Mokov A. S., Voronkov M. G. Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene // Mendeleev Communications. 1995. Vol. 5. No. 2. pp. 53-55.
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Rulev A. Y., Mokov A. S., Voronkov M. G. Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene // Mendeleev Communications. 1995. Vol. 5. No. 2. pp. 53-55.
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TY - JOUR
DO - 10.1070/MC1995v005n02ABEH000454
UR - https://mendcomm.colab.ws/publications/10.1070/MC1995v005n02ABEH000454
TI - Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene
T2 - Mendeleev Communications
AU - Rulev, Alexander Yur'evich
AU - Mokov, Alexander Sergeevich
AU - Voronkov, Mikhail Grigor'evich
PY - 1995
DA - 1995/04/30
PB - Mendeleev Communications
SP - 53-55
IS - 2
VL - 5
ER -
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@article{1995_Rulev,
author = {Alexander Yur'evich Rulev and Alexander Sergeevich Mokov and Mikhail Grigor'evich Voronkov},
title = {Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene},
journal = {Mendeleev Communications},
year = {1995},
volume = {5},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1995v005n02ABEH000454},
number = {2},
pages = {53--55},
doi = {10.1070/MC1995v005n02ABEH000454}
}
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Rulev, Alexander Yur'evich, et al. “Alternative Protonation Centres in the Molecule of 1-(N-Methylimino)-2-(N,N-disubstituted)aminobut-2-ene.” Mendeleev Communications, vol. 5, no. 2, Apr. 1995, pp. 53-55. https://mendcomm.colab.ws/publications/10.1070/MC1995v005n02ABEH000454.

Abstract

The formation of enammonium salts by protonation of azomethine derivatives of N,N-disubstituted α-aminocrotonaldehydes, their easy E,Z-isomerisation and subsequent transformation to the corresponding immonium salts has been found for the first time.

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