Angewandte Chemie - International Edition, volume 57, issue 32, pages 10338-10342
(3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines
Vasin Vladimir S
1
,
Kuznetsov V. V.
2
,
Ivanova Olga
3
,
Shumsky Alexey N
4
,
Makhova Nina N.
2
,
Trushkov Igor V
1, 5
Publication type: Journal Article
Publication date: 2018-07-17
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 16.6
ISSN: 14337851, 15213773
General Chemistry
Catalysis
Abstract
The first example of (3+3)-annulation of two different three-membered rings is reported herein. Donor-acceptor cyclopropanes in reaction with diaziridines were found to afford perhydropyridazine derivatives in high yields and diastereoselectivity under mild Lewis acid catalysis. The disclosed reaction is applicable for the broad substrate scope and exhibits an excellent functional group tolerance.
Citations by journals
2
4
6
8
10
12
14
16
|
|
Organic Letters
|
Organic Letters
15 publications, 15.15%
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
9 publications, 9.09%
|
Angewandte Chemie - International Edition
|
Angewandte Chemie - International Edition
8 publications, 8.08%
|
Angewandte Chemie
|
Angewandte Chemie
8 publications, 8.08%
|
Chemical Communications
|
Chemical Communications
7 publications, 7.07%
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
6 publications, 6.06%
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
6 publications, 6.06%
|
Organic Chemistry Frontiers
|
Organic Chemistry Frontiers
3 publications, 3.03%
|
Mendeleev Communications
|
Mendeleev Communications
3 publications, 3.03%
|
Chemistry - A European Journal
|
Chemistry - A European Journal
3 publications, 3.03%
|
Structural Chemistry
|
Structural Chemistry
2 publications, 2.02%
|
Journal of the American Chemical Society
|
Journal of the American Chemical Society
2 publications, 2.02%
|
Molecules
|
Molecules
2 publications, 2.02%
|
Synlett
|
Synlett
2 publications, 2.02%
|
Molecular Catalysis
|
Molecular Catalysis
2 publications, 2.02%
|
Physical Chemistry Chemical Physics
|
Physical Chemistry Chemical Physics
1 publication, 1.01%
|
Russian Journal of Physical Chemistry A
|
Russian Journal of Physical Chemistry A
1 publication, 1.01%
|
Journal of Physical Chemistry A
|
Journal of Physical Chemistry A
1 publication, 1.01%
|
ChemistrySelect
|
ChemistrySelect
1 publication, 1.01%
|
Chemistry of Heterocyclic Compounds
|
Chemistry of Heterocyclic Compounds
1 publication, 1.01%
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 1.01%
|
Nature Chemistry
|
Nature Chemistry
1 publication, 1.01%
|
Journal of Molecular Structure
|
Journal of Molecular Structure
1 publication, 1.01%
|
Russian Chemical Reviews
|
Russian Chemical Reviews
1 publication, 1.01%
|
Tetrahedron Letters
|
Tetrahedron Letters
1 publication, 1.01%
|
Trends in Chemistry
|
Trends in Chemistry
1 publication, 1.01%
|
Tetrahedron
|
Tetrahedron
1 publication, 1.01%
|
Asian Journal of Organic Chemistry
|
Asian Journal of Organic Chemistry
1 publication, 1.01%
|
Accounts of Chemical Research
|
Accounts of Chemical Research
1 publication, 1.01%
|
2
4
6
8
10
12
14
16
|
Citations by publishers
5
10
15
20
25
30
35
|
|
Wiley
|
Wiley
33 publications, 33.33%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
28 publications, 28.28%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
13 publications, 13.13%
|
Elsevier
|
Elsevier
10 publications, 10.1%
|
Springer Nature
|
Springer Nature
4 publications, 4.04%
|
Pleiades Publishing
|
Pleiades Publishing
2 publications, 2.02%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
2 publications, 2.02%
|
Thieme
|
Thieme
2 publications, 2.02%
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 1.01%
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.01%
|
5
10
15
20
25
30
35
|
- 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":[2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0],"imageUrls":["","","","","","",""],"datasets":[{"label":"Citations number","data":[4,29,21,17,12,12,4],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.04","29.29","21.21","17.17","12.12","12.12","4.04"],"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":["Organic Letters","Journal of Organic Chemistry","Angewandte Chemie - International Edition","Angewandte Chemie","Chemical Communications","European Journal of Organic Chemistry","Advanced Synthesis and Catalysis","Organic Chemistry Frontiers","Mendeleev Communications","Chemistry - A European Journal","Structural Chemistry","Journal of the American Chemical Society","Molecules","Synlett","Molecular Catalysis","Physical Chemistry Chemical Physics","Russian Journal of Physical Chemistry A","Journal of Physical Chemistry A","ChemistrySelect","Chemistry of Heterocyclic Compounds","Beilstein Journal of Organic Chemistry","Nature Chemistry","Journal of Molecular Structure","Russian Chemical Reviews","Tetrahedron Letters","Trends in Chemistry","Tetrahedron","Asian Journal of Organic Chemistry","Accounts of Chemical Research"],"ids":[3315,8697,19215,25450,9073,19472,3906,3991,5294,24708,14347,4813,1770,10217,4906,1773,6134,15255,8021,16828,21928,17228,9347,23802,6133,4660,3439,9409,1526],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_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\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp"],"datasets":[{"label":"","data":[15,9,8,8,7,6,6,3,3,3,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"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","#3B82F6","#3B82F6","#3B82F6"],"percentage":[15.15,9.09,8.08,8.08,7.07,6.06,6.06,3.03,3.03,3.03,2.02,2.02,2.02,2.02,2.02,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01,1.01],"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","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Elsevier","Springer Nature","Pleiades Publishing","Multidisciplinary Digital Publishing Institute (MDPI)","Thieme","Beilstein-Institut","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,8,101,202,135,6139,9422],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[33,28,13,10,4,2,2,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[33.33,28.28,13.13,10.1,4.04,2.02,2.02,2.02,1.01,1.01],"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
Chagarovskiy A. O. et al. (3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines // Angewandte Chemie - International Edition. 2018. Vol. 57. No. 32. pp. 10338-10342.
GOST all authors (up to 50)
Copy
Chagarovskiy A. O., Vasin V. S., Kuznetsov V. V., Ivanova O., Rybakov V. B., Shumsky A. N., Makhova N. N., Trushkov I. V. (3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines // Angewandte Chemie - International Edition. 2018. Vol. 57. No. 32. pp. 10338-10342.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/anie.201805258
UR - https://doi.org/10.1002%2Fanie.201805258
TI - (3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines
T2 - Angewandte Chemie - International Edition
AU - Vasin, Vladimir S
AU - Chagarovskiy, Alexey O
AU - Kuznetsov, V. V.
AU - Ivanova, Olga
AU - Shumsky, Alexey N
AU - Makhova, Nina N.
AU - Trushkov, Igor V
AU - Rybakov, Victor B.
PY - 2018
DA - 2018/07/17 00:00:00
PB - Wiley
SP - 10338-10342
IS - 32
VL - 57
SN - 1433-7851
SN - 1521-3773
ER -
Cite this
BibTex
Copy
@article{2018_Chagarovskiy
author = {Vladimir S Vasin and Alexey O Chagarovskiy and V. V. Kuznetsov and Olga Ivanova and Alexey N Shumsky and Nina N. Makhova and Igor V Trushkov and Victor B. Rybakov},
title = {(3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines},
journal = {Angewandte Chemie - International Edition},
year = {2018},
volume = {57},
publisher = {Wiley},
month = {jul},
url = {https://doi.org/10.1002%2Fanie.201805258},
number = {32},
pages = {10338--10342},
doi = {10.1002/anie.201805258}
}
Cite this
MLA
Copy
Chagarovskiy, Alexey O., et al. “(3+3)-Annulation of Donor–Acceptor Cyclopropanes with Diaziridines.” Angewandte Chemie - International Edition, vol. 57, no. 32, Jul. 2018, pp. 10338-10342. https://doi.org/10.1002%2Fanie.201805258.