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2-Diazoacethydrazide derivatives and their ring-chain transformations

Yurii Aleksandrovich Rosin 1
Yurii Aleksandrovich Rosin
, 
Elena Anatol'evna Vorob'eva 1
Elena Anatol'evna Vorob'eva
, 
Yury Yur'evich Morzherin 2
Yury Yur'evich Morzherin
, 
Alexander S Yakimov 1
Alexander S Yakimov
, 
Wim Dehaen 3
Wim Dehaen
, 
10.1070/MC1998v008n06ABEH001032
Published 1998-12-16
Communication , Volume 8, Issue 6, 240-241
3
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Rosin Y. A. et al. 2-Diazoacethydrazide derivatives and their ring-chain transformations // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 240-241.
GOST all authors (up to 50) Copy
Rosin Y. A., Vorob'eva E. A., Morzherin Y. Y., Yakimov A. S., Dehaen W., Bakulev V. A. 2-Diazoacethydrazide derivatives and their ring-chain transformations // Mendeleev Communications. 1998. Vol. 8. No. 6. pp. 240-241.
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TY - JOUR
DO - 10.1070/MC1998v008n06ABEH001032
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001032
TI - 2-Diazoacethydrazide derivatives and their ring-chain transformations
T2 - Mendeleev Communications
AU - Rosin, Yurii Aleksandrovich
AU - Vorob'eva, Elena Anatol'evna
AU - Morzherin, Yury Yur'evich
AU - Yakimov, Alexander S
AU - Dehaen, Wim
AU - Bakulev, Vasiliy Alekseevich
PY - 1998
DA - 1998/12/16
PB - Mendeleev Communications
SP - 240-241
IS - 6
VL - 8
ER -
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@article{1998_Rosin,
author = {Yurii Aleksandrovich Rosin and Elena Anatol'evna Vorob'eva and Yury Yur'evich Morzherin and Alexander S Yakimov and Wim Dehaen and Vasiliy Alekseevich Bakulev},
title = {2-Diazoacethydrazide derivatives and their ring-chain transformations},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001032},
number = {6},
pages = {240--241},
doi = {10.1070/MC1998v008n06ABEH001032}
}
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Rosin, Yurii Aleksandrovich, et al. “2-Diazoacethydrazide derivatives and their ring-chain transformations.” Mendeleev Communications, vol. 8, no. 6, Dec. 1998, pp. 240-241. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n06ABEH001032.

Abstract

1-Amino-1,2,3-triazol-5-olates 6, 13 and 14 have been obtained by the introduction of a diazo group into N-benzylidene-protected hydrazides of cyanoacetic and malonic acids. These compounds form open-chain isomers of 1-amino-5-hydroxy-1,2,3-triazoles upon acidification with an aqueous solution of HCl. Compounds 8, 15 and 16 are the first examples of the group of α-diazoacethydrazides

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