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Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone

Albina Afanas'evna Tabatskaya 1
Albina Afanas'evna Tabatskaya
Elena F Kutasheva 1
Elena F Kutasheva
Vladislav Mikhailovich Vlasov 1
Vladislav Mikhailovich Vlasov
Published 1993-08-31
CommunicationVolume 3, Issue 4, 163-164
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Tabatskaya A. A., Kutasheva E. F., Vlasov V. M. Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone // Mendeleev Communications. 1993. Vol. 3. No. 4. pp. 163-164.
GOST all authors (up to 50) Copy
Tabatskaya A. A., Kutasheva E. F., Vlasov V. M. Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone // Mendeleev Communications. 1993. Vol. 3. No. 4. pp. 163-164.
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TY - JOUR
DO - 10.1070/MC1993v003n04ABEH000270
UR - https://mendcomm.colab.ws/publications/10.1070/MC1993v003n04ABEH000270
TI - Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone
T2 - Mendeleev Communications
AU - Tabatskaya, Albina Afanas'evna
AU - Kutasheva, Elena F
AU - Vlasov, Vladislav Mikhailovich
PY - 1993
DA - 1993/08/31
PB - Mendeleev Communications
SP - 163-164
IS - 4
VL - 3
ER -
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@article{1993_Tabatskaya,
author = {Albina Afanas'evna Tabatskaya and Elena F Kutasheva and Vladislav Mikhailovich Vlasov},
title = {Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone},
journal = {Mendeleev Communications},
year = {1993},
volume = {3},
publisher = {Mendeleev Communications},
month = {Aug},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1993v003n04ABEH000270},
number = {4},
pages = {163--164},
doi = {10.1070/MC1993v003n04ABEH000270}
}
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Tabatskaya, Albina Afanas'evna, et al. “Reagent Influence on the Direction of Nucleophilic Substitution in 1,4-Nitrochloroanthraquinone.” Mendeleev Communications, vol. 3, no. 4, Aug. 1993, pp. 163-164. https://mendcomm.colab.ws/publications/10.1070/MC1993v003n04ABEH000270.

Abstract

In the reaction of 1,4-nitrochloroanthraquinone with phenoxy anions in DMSO, the main products are those of chlorine substitution, whereas thiophenoxy anions predominantly replace the nitro group

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