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Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines

Nikita Valer'evich Shtyrlin 1
Nikita Valer'evich Shtyrlin
, 
Olga Aleksandrovna Lodochnikova 2
Olga Aleksandrovna Lodochnikova
, 
10.1016/j.mencom.2012.05.021
Published 2012-04-27
Communication , Volume 22, Issue 3, 169-170
17
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Shtyrlin N. V., Lodochnikova O. A., Shtyrlin Y. G. Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines // Mendeleev Communications. 2012. Vol. 22. No. 3. pp. 169-170.
GOST all authors (up to 50) Copy
Shtyrlin N. V., Lodochnikova O. A., Shtyrlin Y. G. Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines // Mendeleev Communications. 2012. Vol. 22. No. 3. pp. 169-170.
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TY - JOUR
DO - 10.1016/j.mencom.2012.05.021
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.021
TI - Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines
T2 - Mendeleev Communications
AU - Shtyrlin, Nikita Valer'evich
AU - Lodochnikova, Olga Aleksandrovna
AU - Shtyrlin, Yurii Grigor'evich
PY - 2012
DA - 2012/04/27
PB - Mendeleev Communications
SP - 169-170
IS - 3
VL - 22
ER -
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@article{2012_Shtyrlin,
author = {Nikita Valer'evich Shtyrlin and Olga Aleksandrovna Lodochnikova and Yurii Grigor'evich Shtyrlin},
title = {Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.021},
number = {3},
pages = {169--170},
doi = {10.1016/j.mencom.2012.05.021}
}
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Shtyrlin, Nikita Valer'evich, et al. “Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines.” Mendeleev Communications, vol. 22, no. 3, Apr. 2012, pp. 169-170. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.021.

Abstract

The selective oxidation of 2- and 4-positioned hydroxymethyl groups of 6-methyl-2,3,4-tris(hydroxymethyl)pyridin-5-ol was developed and the thus obtained aldehydes were converted into their oximes and thiosemicarbazones.

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