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Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene

Oleg Yuryevich Sapozhnikov 1
Oleg Yuryevich Sapozhnikov
Elena V Smirnova 1
Elena V Smirnova
Mikhail Dmitrievich Dutov 1
Mikhail Dmitrievich Dutov
Vadim Vadimovich Kachala 1
Vadim Vadimovich Kachala
Published 2005-09-09
CommunicationVolume 15, Issue 5, 200-202
9
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Sapozhnikov O. Y. et al. Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene // Mendeleev Communications. 2005. Vol. 15. No. 5. pp. 200-202.
GOST all authors (up to 50) Copy
Sapozhnikov O. Y., Smirnova E. V., Dutov M. D., Kachala V. V. Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene // Mendeleev Communications. 2005. Vol. 15. No. 5. pp. 200-202.
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TY - JOUR
DO - 10.1070/MC2005v015n05ABEH002128
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002128
TI - Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene
T2 - Mendeleev Communications
AU - Sapozhnikov, Oleg Yuryevich
AU - Smirnova, Elena V
AU - Dutov, Mikhail Dmitrievich
AU - Kachala, Vadim Vadimovich
PY - 2005
DA - 2005/09/09
PB - Mendeleev Communications
SP - 200-202
IS - 5
VL - 15
ER -
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@article{2005_Sapozhnikov,
author = {Oleg Yuryevich Sapozhnikov and Elena V Smirnova and Mikhail Dmitrievich Dutov and Vadim Vadimovich Kachala},
title = {Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002128},
number = {5},
pages = {200--202},
doi = {10.1070/MC2005v015n05ABEH002128}
}
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Sapozhnikov, Oleg Yuryevich, et al. “Synthesis of 4-substituted 6-dinitrobenzo[d]isothiazoles from 2,4,6-trinitrotoluene.” Mendeleev Communications, vol. 15, no. 5, Sep. 2005, pp. 200-202. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n05ABEH002128.

Abstract

The synthesis of 4,6-dinitrobenzo[d]isothiazole from a product obtained by the replacement of the ortho-NO2 group in N-2,4,6-trinitrobenzylidene-4’-N,N-dimethylaminoaniline on treatment with PhCH2SH was developed.

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