Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles
Boris V Lyalin
1
,
Vera L Sigacheva
1
,
Anastasia S Kudinova
1
,
Bogdan I. Ugrak
1
,
Vladimir A Petrosyan
1
,
Vladimir A Kokorekin
1, 2, 3
Publication type: Journal Article
Publication date: 2022-01-01
scimago Q4
wos Q4
SJR: 0.243
CiteScore: 2.7
Impact factor: 1.0
ISSN: 00093122, 15738353
Organic Chemistry
Abstract
In this article, we showed N–N cross coupling of 4-(un)substituted 1-alkyl-3-aminopyrazoles using electrogenerated reagents (NiO(OH), NaOCl, NaOBr, or Br2) for the first time. It was found that the oxidation potentials of the initial azoles reflect their reactivity and are the key factors in the efficiency of the target and side processes. This made it possible to identify suitable combinations of azoles and electrogenerated reagents and to obtain unsymmetrical azo compounds under mild conditions in aqueous media with 48–83% yields.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
|
|
|
Mendeleev Communications
1 publication, 25%
|
|
|
Green Chemistry
1 publication, 25%
|
|
|
Structural Chemistry
1 publication, 25%
|
|
|
Energetic Materials Frontiers
1 publication, 25%
|
|
|
1
|
Publishers
|
1
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 publication, 25%
|
|
|
Royal Society of Chemistry (RSC)
1 publication, 25%
|
|
|
Springer Nature
1 publication, 25%
|
|
|
Elsevier
1 publication, 25%
|
|
|
1
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
4
Total citations:
4
Citations from 2025:
3
(75%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Lyalin B. V. et al. Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles // Chemistry of Heterocyclic Compounds. 2022. Vol. 58. No. 1. pp. 1-6.
GOST all authors (up to 50)
Copy
Lyalin B. V., Sigacheva V. L., Kudinova A. S., Ugrak B. I., Petrosyan V. A., Kokorekin V. A. Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles // Chemistry of Heterocyclic Compounds. 2022. Vol. 58. No. 1. pp. 1-6.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s10593-022-03049-y
UR - https://doi.org/10.1007/s10593-022-03049-y
TI - Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles
T2 - Chemistry of Heterocyclic Compounds
AU - Lyalin, Boris V
AU - Sigacheva, Vera L
AU - Kudinova, Anastasia S
AU - Ugrak, Bogdan I.
AU - Petrosyan, Vladimir A
AU - Kokorekin, Vladimir A
PY - 2022
DA - 2022/01/01
PB - Springer Nature
SP - 1-6
IS - 1
VL - 58
SN - 0009-3122
SN - 1573-8353
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2022_Lyalin,
author = {Boris V Lyalin and Vera L Sigacheva and Anastasia S Kudinova and Bogdan I. Ugrak and Vladimir A Petrosyan and Vladimir A Kokorekin},
title = {Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles},
journal = {Chemistry of Heterocyclic Compounds},
year = {2022},
volume = {58},
publisher = {Springer Nature},
month = {jan},
url = {https://doi.org/10.1007/s10593-022-03049-y},
number = {1},
pages = {1--6},
doi = {10.1007/s10593-022-03049-y}
}
Cite this
MLA
Copy
Lyalin, Boris V., et al. “Electrooxidative N–N Cross Coupling: A Way to New Azopyrazoles.” Chemistry of Heterocyclic Compounds, vol. 58, no. 1, Jan. 2022, pp. 1-6. https://doi.org/10.1007/s10593-022-03049-y.