Chemistry of Heterocyclic Compounds, volume 53, issue 6-7, pages 670-681
Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides
1
2
Foreign Limited Liability Company BASF, Minsk, Belarus
|
Publication type: Journal Article
Publication date: 2017-06-01
Journal:
Chemistry of Heterocyclic Compounds
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.5
ISSN: 00093122, 15738353
Organic Chemistry
Abstract
This review provides comprehensive analysis of literature data on the heterocyclization reaction of primary amines, orthoesters, and azides, which can be used for the preparation of tetrazole, its 1-mono- and 1,5-disubstituted derivatives.
Top-30
Citations by journals
1
2
|
|
Polyhedron
2 publications, 8.33%
|
|
Zeitschrift fur Anorganische und Allgemeine Chemie
2 publications, 8.33%
|
|
ChemistrySelect
2 publications, 8.33%
|
|
Frontiers in Chemistry
1 publication, 4.17%
|
|
Chemistry of Heterocyclic Compounds
1 publication, 4.17%
|
|
Russian Chemical Bulletin
1 publication, 4.17%
|
|
Journal of Solid State Chemistry
1 publication, 4.17%
|
|
Journal of Physics: Conference Series
1 publication, 4.17%
|
|
Mendeleev Communications
1 publication, 4.17%
|
|
Molecular Catalysis
1 publication, 4.17%
|
|
Inorganica Chimica Acta
1 publication, 4.17%
|
|
Chemistry - An Asian Journal
1 publication, 4.17%
|
|
Asian Journal of Organic Chemistry
1 publication, 4.17%
|
|
Journal of Organic Chemistry
1 publication, 4.17%
|
|
Journal of Materials Chemistry A
1 publication, 4.17%
|
|
Dalton Transactions
1 publication, 4.17%
|
|
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
1 publication, 4.17%
|
|
Journal of the Belarusian State University Chemistry
1 publication, 4.17%
|
|
Advances in Heterocyclic Chemistry
1 publication, 4.17%
|
|
Russian Chemical Reviews
1 publication, 4.17%
|
|
1
2
|
Citations by publishers
1
2
3
4
5
6
7
|
|
Elsevier
7 publications, 29.17%
|
|
Wiley
6 publications, 25%
|
|
Springer Nature
2 publications, 8.33%
|
|
Royal Society of Chemistry (RSC)
2 publications, 8.33%
|
|
Frontiers Media S.A.
1 publication, 4.17%
|
|
IOP Publishing
1 publication, 4.17%
|
|
American Chemical Society (ACS)
1 publication, 4.17%
|
|
Pleiades Publishing
1 publication, 4.17%
|
|
Belarusian State University
1 publication, 4.17%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 4.17%
|
|
1
2
3
4
5
6
7
|
- We do not take into account publications 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":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,4,4,4,3,5,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.17","16.67","16.67","16.67","12.5","20.83","8.33","4.17"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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":["Polyhedron","Zeitschrift fur Anorganische und Allgemeine Chemie","ChemistrySelect","Frontiers in Chemistry","Chemistry of Heterocyclic Compounds","Russian Chemical Bulletin","Journal of Solid State Chemistry","Journal of Physics: Conference Series","Mendeleev Communications","Molecular Catalysis","Inorganica Chimica Acta","Chemistry - An Asian Journal","Asian Journal of Organic Chemistry","Journal of Organic Chemistry","Journal of Materials Chemistry A","Dalton Transactions","Russian Journal of Coordination Chemistry\/Koordinatsionnaya Khimiya","Journal of the Belarusian State University Chemistry","Advances in Heterocyclic Chemistry","Russian Chemical Reviews"],"ids":[21269,18677,8021,6407,16828,10918,2684,3333,5294,4906,1406,10120,9409,8697,14919,8473,12054,28256,7227,23802],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/LsKy6OnmmmRGcAU6CZgWQvNiP1polbaSLNrN7zqj_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/hnERrPYgmXBUc18M9koKPiDBSTAVjRClgZsf3hqi_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[8.33,8.33,8.33,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17,4.17],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"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","Wiley","Springer Nature","Royal Society of Chemistry (RSC)","Frontiers Media S.A.","IOP Publishing","American Chemical Society (ACS)","Pleiades Publishing","Belarusian State University","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[17,11,8,123,208,2075,40,101,7522,9422],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/LsKy6OnmmmRGcAU6CZgWQvNiP1polbaSLNrN7zqj_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/hnERrPYgmXBUc18M9koKPiDBSTAVjRClgZsf3hqi_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[7,6,2,2,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[29.17,25,8.33,8.33,4.17,4.17,4.17,4.17,4.17,4.17],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":false}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartiles":{"type":"bar","data":{"show":true,"labels":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[1,1,0,1,0,2,1,0],"percentage":["4.17","4.17","0","4.17","0","8.33","4.17","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,2,3,2,0,1,0],"percentage":["0","0","8.33","12.5","8.33","0","4.17","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,3,1,0,0,1,0,1],"percentage":["0","12.5","4.17","0","0","4.17","0","4.17"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,1,0,1,2,0,0],"percentage":["0","0","4.17","0","4.17","8.33","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by SCImago per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartilesWs":{"type":"bar","data":{"show":true,"labels":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[1,0,0,0,0,1,0,0],"percentage":["4.17","0","0","0","0","4.17","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,1,2,0,1,1,0],"percentage":["0","4.17","4.17","8.33","0","4.17","4.17","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,2,1,2,2,0,1,0],"percentage":["0","8.33","4.17","8.33","8.33","0","4.17","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,1,0,0,1,0,1],"percentage":["0","4.17","4.17","0","0","4.17","0","4.17"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,1,0,1,2,0,0],"percentage":["0","0","4.17","0","4.17","8.33","0","0"]}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"},"stacked":true}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations quartiles by WoS per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Grigoriev Y. V. et al. Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides // Chemistry of Heterocyclic Compounds. 2017. Vol. 53. No. 6-7. pp. 670-681.
GOST all authors (up to 50)
Copy
Grigoriev Y. V., Voitekhovich S. V., Karavai V. P., Ivashkevich O. A. Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides // Chemistry of Heterocyclic Compounds. 2017. Vol. 53. No. 6-7. pp. 670-681.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1007/s10593-017-2108-7
UR - https://doi.org/10.1007/s10593-017-2108-7
TI - Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides
T2 - Chemistry of Heterocyclic Compounds
AU - Grigoriev, Yurii V
AU - Voitekhovich, Sergei V
AU - Karavai, Vladimir P
AU - Ivashkevich, Oleg A
PY - 2017
DA - 2017/06/01 00:00:00
PB - Springer Nature
SP - 670-681
IS - 6-7
VL - 53
SN - 0009-3122
SN - 1573-8353
ER -
Cite this
BibTex
Copy
@article{2017_Grigoriev,
author = {Yurii V Grigoriev and Sergei V Voitekhovich and Vladimir P Karavai and Oleg A Ivashkevich},
title = {Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides},
journal = {Chemistry of Heterocyclic Compounds},
year = {2017},
volume = {53},
publisher = {Springer Nature},
month = {jun},
url = {https://doi.org/10.1007/s10593-017-2108-7},
number = {6-7},
pages = {670--681},
doi = {10.1007/s10593-017-2108-7}
}
Cite this
MLA
Copy
Grigoriev, Yurii V., et al. “Synthesis of tetrazole and its derivatives by heterocyclization reaction involving primary amines, orthoesters, and azides.” Chemistry of Heterocyclic Compounds, vol. 53, no. 6-7, Jun. 2017, pp. 670-681. https://doi.org/10.1007/s10593-017-2108-7.