Mendeleev Communications, volume 25, issue 6, pages 399-409
Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems
Publication type: Journal Article
Publication date: 2015-11-01
Journal:
Mendeleev Communications
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.9
ISSN: 09599436, 1364551X
General Chemistry
Abstract
Organic compounds bearing semi-polar nitrogen–oxygen bonds are considered as perspective platform for designing socially important medications and high energy materials. Herein, recently developed original syntheses of monocyclic and fused 1,2,3,4-tetrazine 1,3-dioxides, various (methylene)bis(1-oxy-1-triazene 2-oxide) derivatives, furoxan-containing polyheterocyclic scaffolds and diastereoor enantiomerically enriched functionalized aliphatic nitro compounds are summarized. Prospects for their practical applications are outlined.
Citations by journals
|
5
10
15
20
|
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
20 publications, 31.75%
|
|
Mendeleev Communications
|
Mendeleev Communications
15 publications, 23.81%
|
|
Tetrahedron Letters
|
Tetrahedron Letters
4 publications, 6.35%
|
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
3 publications, 4.76%
|
|
ChemPlusChem
|
ChemPlusChem
1 publication, 1.59%
|
|
RSC Advances
|
RSC Advances
1 publication, 1.59%
|
|
ChemSusChem
|
ChemSusChem
1 publication, 1.59%
|
|
ChemMedChem
|
ChemMedChem
1 publication, 1.59%
|
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 1.59%
|
|
ACS Catalysis
|
ACS Catalysis
1 publication, 1.59%
|
|
Organic and Biomolecular Chemistry
|
Organic and Biomolecular Chemistry
1 publication, 1.59%
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 1.59%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 1.59%
|
|
Journal of Chemical Physics
|
Journal of Chemical Physics
1 publication, 1.59%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 1.59%
|
|
Molecular Diversity
|
Molecular Diversity
1 publication, 1.59%
|
|
Steroids
|
Steroids
1 publication, 1.59%
|
|
Tetrahedron
|
Tetrahedron
1 publication, 1.59%
|
|
ChemInform
|
ChemInform
1 publication, 1.59%
|
|
Angewandte Chemie - International Edition
|
Angewandte Chemie - International Edition
1 publication, 1.59%
|
|
Angewandte Chemie
|
Angewandte Chemie
1 publication, 1.59%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 1.59%
|
|
Progress in Heterocyclic Chemistry
|
Progress in Heterocyclic Chemistry
1 publication, 1.59%
|
|
Synthesis
|
Synthesis
1 publication, 1.59%
|
|
Chemical Biology and Drug Design
|
Chemical Biology and Drug Design
1 publication, 1.59%
|
|
5
10
15
20
|
Citations by publishers
|
5
10
15
20
25
|
|
|
Elsevier
|
Elsevier
22 publications, 34.92%
|
|
Springer Nature
|
Springer Nature
22 publications, 34.92%
|
|
Wiley
|
Wiley
11 publications, 17.46%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 3.17%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
2 publications, 3.17%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.59%
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 1.59%
|
|
American Institute of Physics (AIP)
|
American Institute of Physics (AIP)
1 publication, 1.59%
|
|
Thieme
|
Thieme
1 publication, 1.59%
|
|
5
10
15
20
25
|
- 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":[2016,2017,2018,2019,2020,2021,2022,2023],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[25,23,9,1,2,0,0,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["39.68","36.51","14.29","1.59","3.17",0,0,"4.76"],"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":["Russian Chemical Bulletin","Mendeleev Communications","Tetrahedron Letters","European Journal of Organic Chemistry","ChemPlusChem","RSC Advances","ChemSusChem","ChemMedChem","Russian Chemical Reviews","ACS Catalysis","Organic and Biomolecular Chemistry","Journal of Organic Chemistry","Beilstein Journal of Organic Chemistry","Journal of Chemical Physics","Chemistry of Heterocyclic Compounds","Molecular Diversity","Steroids","Tetrahedron","ChemInform","Angewandte Chemie - International Edition","Angewandte Chemie","ChemistrySelect","Progress in Heterocyclic Chemistry","Synthesis","Chemical Biology and Drug Design"],"ids":[10918,5294,6133,19472,21067,3100,6896,1430,23802,4873,541,8697,21928,544,16828,9362,2239,3439,25372,19215,25450,8021,17224,10934,3569],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/ARM4e6URKRsbRZvIF0vFis9DjxGloBjnBYJXbHmZ_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp"],"datasets":[{"label":"","data":[20,15,4,3,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[31.75,23.81,6.35,4.76,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59,1.59],"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","Wiley","Royal Society of Chemistry (RSC)","American Chemical Society (ACS)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Beilstein-Institut","American Institute of Physics (AIP)","Thieme"],"ids":[17,8,11,123,40,9422,6139,250,135],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/ARM4e6URKRsbRZvIF0vFis9DjxGloBjnBYJXbHmZ_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp"],"datasets":[{"label":"","data":[22,22,11,2,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[34.92,34.92,17.46,3.17,3.17,1.59,1.59,1.59,1.59],"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
Khrustalev V. N. et al. Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems // Mendeleev Communications. 2015. Vol. 25. No. 6. pp. 399-409.
GOST all authors (up to 50)
Copy
Khrustalev V. N., Churakov A. M., Lukyanov O. A., Makhova N. N., Sukhorukov A. Yu., Tartakovsky V. A. Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems // Mendeleev Communications. 2015. Vol. 25. No. 6. pp. 399-409.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.mencom.2015.11.001
UR - https://doi.org/10.1016%2Fj.mencom.2015.11.001
TI - Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems
T2 - Mendeleev Communications
AU - Churakov, Aleksandr M
AU - Lukyanov, Oleg A
AU - Tartakovsky, Vladimir A
AU - Khrustalev, Victor N.
AU - Makhova, Nina N.
AU - Sukhorukov, Alexey Yu
PY - 2015
DA - 2015/11/01 00:00:00
PB - Elsevier
SP - 399-409
IS - 6
VL - 25
SN - 0959-9436
SN - 1364-551X
ER -
Cite this
BibTex
Copy
@article{2015_Khrustalev,
author = {Aleksandr M Churakov and Oleg A Lukyanov and Vladimir A Tartakovsky and Victor N. Khrustalev and Nina N. Makhova and Alexey Yu Sukhorukov},
title = {Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Elsevier},
month = {nov},
url = {https://doi.org/10.1016%2Fj.mencom.2015.11.001},
number = {6},
pages = {399--409},
doi = {10.1016/j.mencom.2015.11.001}
}
Cite this
MLA
Copy
Khrustalev, Victor N., et al. “Novel approaches to pharmacology-oriented and energy rich organic nitrogen-oxygen systems.” Mendeleev Communications, vol. 25, no. 6, Nov. 2015, pp. 399-409. https://doi.org/10.1016%2Fj.mencom.2015.11.001.
Profiles