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Nucleophilic substitution in azasydnone-modified dinitroanisoles

Tatiana Konstantinovna Shkineva 1
Tatiana Konstantinovna Shkineva
Alexander Vasilyvich Kormanov 1
Alexander Vasilyvich Kormanov
Igor L'vovich Dalinger 1
Igor L'vovich Dalinger
Published 2025-03-31
CommunicationVolume 35, Issue 3, 271-273
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Shkineva T. K., Kormanov A. V., Dalinger I. L. Nucleophilic substitution in azasydnone-modified dinitroanisoles // Mendeleev Communications. 2025. Vol. 35. No. 3. pp. 271-273.
GOST all authors (up to 50) Copy
Shkineva T. K., Kormanov A. V., Dalinger I. L. Nucleophilic substitution in azasydnone-modified dinitroanisoles // Mendeleev Communications. 2025. Vol. 35. No. 3. pp. 271-273.
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TY - JOUR
DO - 10.71267/mencom.7614
UR - https://mendcomm.colab.ws/publications/10.71267/mencom.7614
TI - Nucleophilic substitution in azasydnone-modified dinitroanisoles
T2 - Mendeleev Communications
AU - Shkineva, Tatiana Konstantinovna
AU - Kormanov, Alexander Vasilyvich
AU - Dalinger, Igor L'vovich
PY - 2025
DA - 2025/03/31
PB - Mendeleev Communications
SP - 271-273
IS - 3
VL - 35
ER -
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@article{2025_Shkineva,
author = {Tatiana Konstantinovna Shkineva and Alexander Vasilyvich Kormanov and Igor L'vovich Dalinger},
title = {Nucleophilic substitution in azasydnone-modified dinitroanisoles},
journal = {Mendeleev Communications},
year = {2025},
volume = {35},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.71267/mencom.7614},
number = {3},
pages = {271--273},
doi = {10.71267/mencom.7614}
}
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Shkineva, Tatiana Konstantinovna, et al. “Nucleophilic substitution in azasydnone-modified dinitroanisoles.” Mendeleev Communications, vol. 35, no. 3, Mar. 2025, pp. 271-273. https://mendcomm.colab.ws/publications/10.71267/mencom.7614.

Keywords

1,2,3,4-oxatriazolium-5-olate
azasydnones
dinitroanilines
dinitroanisoles
mesoionic compounds
methoxy group, benzo[d][1,2,3]triazole 3-oxide
nitrogen rich heterocycles
nucleophilic substitution

Abstract

Reactions of 3-(4-methoxy-3,5-dinitrophenyl)-1,2,3,4-oxatriazolium-5-olate with N-nucleophiles under mild conditions results in the displacement of the methoxy group leaving 1,2,3,4-oxatriazolium-5-olate (azasydnone) moiety intact. In the case of alkylhydrazines, further cyclization involving nitro group into benzo[d][1,2,3]triazole 3-oxides occurs.

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