Home / Publications / Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles

Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles

Evgeniy Viktorovich Tret'yakov 1
Evgeniy Viktorovich Tret'yakov
Sergey Franzevich Vasilevskii 1
Sergey Franzevich Vasilevskii
Published 1995-12-31
CommunicationVolume 5, Issue 6, 233-234
12
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Tret'yakov E. V., Vasilevskii S. F. Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles // Mendeleev Communications. 1995. Vol. 5. No. 6. pp. 233-234.
GOST all authors (up to 50) Copy
Tret'yakov E. V., Vasilevskii S. F. Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles // Mendeleev Communications. 1995. Vol. 5. No. 6. pp. 233-234.
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TY - JOUR
DO - 10.1070/MC1995v005n06ABEH000542
UR - https://mendcomm.colab.ws/publications/10.1070/MC1995v005n06ABEH000542
TI - Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles
T2 - Mendeleev Communications
AU - Tret'yakov, Evgeniy Viktorovich
AU - Vasilevskii, Sergey Franzevich
PY - 1995
DA - 1995/12/31
PB - Mendeleev Communications
SP - 233-234
IS - 6
VL - 5
ER -
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@article{1995_Tret'yakov,
author = {Evgeniy Viktorovich Tret'yakov and Sergey Franzevich Vasilevskii},
title = {Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles},
journal = {Mendeleev Communications},
year = {1995},
volume = {5},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1995v005n06ABEH000542},
number = {6},
pages = {233--234},
doi = {10.1070/MC1995v005n06ABEH000542}
}
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Tret'yakov, Evgeniy Viktorovich, and Sergey Franzevich Vasilevskii. “Nitrodeiodination of Polyiodopyrazoles: a Convenient Synthesis of 4-Nitroiodopyrazoles.” Mendeleev Communications, vol. 5, no. 6, Dec. 1995, pp. 233-234. https://mendcomm.colab.ws/publications/10.1070/MC1995v005n06ABEH000542.

Abstract

A number of 3,4-, 4,5-diiodo- and 3,4,5-triiodo-1-methylpyrazoles 2a–f have been converted into the corresponding almost inaccessible 3-, 5-iodo- and 3,5-diiodo-1-methyl-4-nitropyrazoles 3a–f by nitration with an HNO3–H2SO4 mixture.

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