Russian Chemical Reviews, volume 80, issue 11, pages 1035-1066
Transformations of diaziridines and their fused analogues induced by electrophilic reagents
Publication type: Journal Article
Publication date: 2011-11-30
Journal:
Russian Chemical Reviews
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 7.7
ISSN: 0036021X, 14684837
General Chemistry
Abstract
The review deals with transformations of mono- and bicyclic diaziridine derivatives with different types of substitution induced by electrophilic reagents (protic acids, Lewis acids, alkylating and acylating agents, carbonyl compounds, heterocumulenes, activated alkenes and alkynes and transition metal salts). The characteristic features of the reactions are considered as functions of the structures of the starting diaziridines and the nature of the reaction medium (organic solvents, ionic liquids). Prospects of the use of diaziridine derivatives as readily available precursors for the synthesis of various nitrogen-containing heterocyclic systems based on the diaziridine ring expansion reactions are considered. The bibliography includes 136 references.
Citations by journals
|
1
2
3
4
5
|
|
|
Mendeleev Communications
|
Mendeleev Communications
5 publications, 11.36%
|
|
Angewandte Chemie - International Edition
|
Angewandte Chemie - International Edition
3 publications, 6.82%
|
|
Structural Chemistry
|
Structural Chemistry
3 publications, 6.82%
|
|
Angewandte Chemie
|
Angewandte Chemie
3 publications, 6.82%
|
|
Organic Letters
|
Organic Letters
3 publications, 6.82%
|
|
Journal of Molecular Structure
|
Journal of Molecular Structure
2 publications, 4.55%
|
|
Physical Chemistry Chemical Physics
|
Physical Chemistry Chemical Physics
2 publications, 4.55%
|
|
Tetrahedron
|
Tetrahedron
2 publications, 4.55%
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
2 publications, 4.55%
|
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
2 publications, 4.55%
|
|
Russian Journal of Physical Chemistry A
|
Russian Journal of Physical Chemistry A
1 publication, 2.27%
|
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
1 publication, 2.27%
|
|
Journal of Physical Chemistry A
|
Journal of Physical Chemistry A
1 publication, 2.27%
|
|
ChemistrySelect
|
ChemistrySelect
1 publication, 2.27%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 2.27%
|
|
Molecules
|
Molecules
1 publication, 2.27%
|
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 2.27%
|
|
Journal of Physical Organic Chemistry
|
Journal of Physical Organic Chemistry
1 publication, 2.27%
|
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
1 publication, 2.27%
|
|
ChemInform
|
ChemInform
1 publication, 2.27%
|
|
Chirality
|
Chirality
1 publication, 2.27%
|
|
Journal of the American Chemical Society
|
Journal of the American Chemical Society
1 publication, 2.27%
|
|
Chemical Reviews
|
Chemical Reviews
1 publication, 2.27%
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
1 publication, 2.27%
|
|
Advances in Heterocyclic Chemistry
|
Advances in Heterocyclic Chemistry
1 publication, 2.27%
|
|
Chemical Physics
|
Chemical Physics
1 publication, 2.27%
|
|
1
2
3
4
5
|
Citations by publishers
|
2
4
6
8
10
12
|
|
|
Wiley
|
Wiley
12 publications, 27.27%
|
|
Elsevier
|
Elsevier
11 publications, 25%
|
|
Springer Nature
|
Springer Nature
7 publications, 15.91%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
7 publications, 15.91%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
2 publications, 4.55%
|
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 2.27%
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 2.27%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 2.27%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.27%
|
|
2
4
6
8
10
12
|
- 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":[2,6,5,1,1,1,5,5,4,6,5,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.55","13.64","11.36","2.27","2.27","2.27","11.36","11.36","9.09","13.64","11.36","4.55","2.27"],"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":["Mendeleev Communications","Angewandte Chemie - International Edition","Structural Chemistry","Angewandte Chemie","Organic Letters","Journal of Molecular Structure","Physical Chemistry Chemical Physics","Tetrahedron","Russian Chemical Bulletin","Chemistry of Heterocyclic Compounds","Russian Journal of Physical Chemistry A","European Journal of Organic Chemistry","Journal of Physical Chemistry A","ChemistrySelect","Beilstein Journal of Organic Chemistry","Molecules","Russian Chemical Reviews","Journal of Physical Organic Chemistry","Advanced Synthesis and Catalysis","ChemInform","Chirality","Journal of the American Chemical Society","Chemical Reviews","Journal of Organic Chemistry","Advances in Heterocyclic Chemistry","Chemical Physics"],"ids":[5294,19215,14347,25450,3315,9347,1773,3439,10918,16828,6134,19472,15255,8021,21928,1770,23802,16036,3906,25372,9710,4813,13718,8697,7227,11321],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[5,3,3,3,3,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"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","#3B82F6"],"percentage":[11.36,6.82,6.82,6.82,6.82,4.55,4.55,4.55,4.55,4.55,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27,2.27],"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":["Wiley","Elsevier","Springer Nature","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Pleiades Publishing","Beilstein-Institut","Multidisciplinary Digital Publishing Institute (MDPI)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,17,8,40,123,101,6139,202,9422],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[12,11,7,7,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[27.27,25,15.91,15.91,4.55,2.27,2.27,2.27,2.27],"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
Makhova N. N., Shevtsov A. V., Petukhova V. Y. Transformations of diaziridines and their fused analogues induced by electrophilic reagents // Russian Chemical Reviews. 2011. Vol. 80. No. 11. pp. 1035-1066.
GOST all authors (up to 50)
Copy
Makhova N. N., Shevtsov A. V., Petukhova V. Y. Transformations of diaziridines and their fused analogues induced by electrophilic reagents // Russian Chemical Reviews. 2011. Vol. 80. No. 11. pp. 1035-1066.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1070/RC2011v080n11ABEH004254
UR - https://doi.org/10.1070%2FRC2011v080n11ABEH004254
TI - Transformations of diaziridines and their fused analogues induced by electrophilic reagents
T2 - Russian Chemical Reviews
AU - Makhova, Nina N
AU - Shevtsov, Alexander V.
AU - Petukhova, Vera Yu.
PY - 2011
DA - 2011/11/30 00:00:00
PB - Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
SP - 1035-1066
IS - 11
VL - 80
SN - 0036-021X
SN - 1468-4837
ER -
Cite this
BibTex
Copy
@article{2011_Makhova,
author = {Nina N Makhova and Alexander V. Shevtsov and Vera Yu. Petukhova},
title = {Transformations of diaziridines and their fused analogues induced by electrophilic reagents},
journal = {Russian Chemical Reviews},
year = {2011},
volume = {80},
publisher = {Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii},
month = {nov},
url = {https://doi.org/10.1070%2FRC2011v080n11ABEH004254},
number = {11},
pages = {1035--1066},
doi = {10.1070/RC2011v080n11ABEH004254}
}
Cite this
MLA
Copy
Makhova, Nina N., et al. “Transformations of diaziridines and their fused analogues induced by electrophilic reagents.” Russian Chemical Reviews, vol. 80, no. 11, Nov. 2011, pp. 1035-1066. https://doi.org/10.1070%2FRC2011v080n11ABEH004254.