Russian Chemical Bulletin, volume 58, issue 12, pages 2474-2477
4-formylsydnonimine derivatives
Publication type: Journal Article
Publication date: 2009-12-01
Journal:
Russian Chemical Bulletin
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.7
ISSN: 10665285, 15739171
General Chemistry
Abstract
The procedure for the synthesis of 4-formylsydnonimine derivatives based on the reaction of 4-lithiosydnonimines with (methoxymethylidene)dimethylammonium methyl sulfate was proposed.
Citations by journals
1
2
|
|
Tetrahedron Letters
|
Tetrahedron Letters
2 publications, 20%
|
Journal of Organometallic Chemistry
|
Journal of Organometallic Chemistry
2 publications, 20%
|
Advances in Heterocyclic Chemistry
|
Advances in Heterocyclic Chemistry
1 publication, 10%
|
Tetrahedron
|
Tetrahedron
1 publication, 10%
|
RSC Advances
|
RSC Advances
1 publication, 10%
|
Agrochemicals
|
Agrochemicals
1 publication, 10%
|
Topics in Heterocyclic Chemistry
|
Topics in Heterocyclic Chemistry
1 publication, 10%
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
1 publication, 10%
|
1
2
|
Citations by publishers
1
2
3
4
5
6
|
|
Elsevier
|
Elsevier
6 publications, 60%
|
Springer Nature
|
Springer Nature
2 publications, 20%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 10%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 10%
|
1
2
3
4
5
6
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,0,0,0,0,0,2,2,1,1,0,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["10",0,0,0,0,0,"20","20","10","10",0,"20","10"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Tetrahedron Letters","Journal of Organometallic Chemistry","Advances in Heterocyclic Chemistry","Tetrahedron","RSC Advances","Agrochemicals","Topics in Heterocyclic Chemistry","Russian Chemical Bulletin"],"ids":[6133,11834,7227,3439,3100,29867,38323,10918],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp"],"datasets":[{"label":"","data":[2,2,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[20,20,10,10,10,10,10,10],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Elsevier","Springer Nature","Royal Society of Chemistry (RSC)","Multidisciplinary Digital Publishing Institute (MDPI)"],"ids":[17,8,123,202],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp"],"datasets":[{"label":"","data":[6,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[60,20,10,10],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Cherepanov I. A. et al. 4-formylsydnonimine derivatives // Russian Chemical Bulletin. 2009. Vol. 58. No. 12. pp. 2474-2477.
GOST all authors (up to 50)
Copy
Cherepanov I. A., Kusaeva L. H., Godovikov I. A., Kalinin V. 4-formylsydnonimine derivatives // Russian Chemical Bulletin. 2009. Vol. 58. No. 12. pp. 2474-2477.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s11172-009-0346-2
UR - https://doi.org/10.1007%2Fs11172-009-0346-2
TI - 4-formylsydnonimine derivatives
T2 - Russian Chemical Bulletin
AU - Cherepanov, I. A.
AU - Kusaeva, L H
AU - Godovikov, I A
AU - Kalinin, V.N.
PY - 2009
DA - 2009/12/01 00:00:00
PB - Springer Nature
SP - 2474-2477
IS - 12
VL - 58
SN - 1066-5285
SN - 1573-9171
ER -
Cite this
BibTex
Copy
@article{2009_Cherepanov,
author = {I. A. Cherepanov and L H Kusaeva and I A Godovikov and V.N. Kalinin},
title = {4-formylsydnonimine derivatives},
journal = {Russian Chemical Bulletin},
year = {2009},
volume = {58},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007%2Fs11172-009-0346-2},
number = {12},
pages = {2474--2477},
doi = {10.1007/s11172-009-0346-2}
}
Cite this
MLA
Copy
Cherepanov, I. A., et al. “4-formylsydnonimine derivatives.” Russian Chemical Bulletin, vol. 58, no. 12, Dec. 2009, pp. 2474-2477. https://doi.org/10.1007%2Fs11172-009-0346-2.
Profiles