European Journal of Organic Chemistry, volume 2008, issue 31, pages 5329-5335
Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes
Publication type: Journal Article
Publication date: 2008-11-01
Quartile SCImago
Q2
Quartile WOS
Q2
Impact factor: 2.8
ISSN: 1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
The reactions of 2-aryl-1,1-cyclopropane diesters with anthracene derivatives were studied for the first time. Three kinds of reaction products are formed depending on the nature of the aryl group and the substituents in the anthracene. The first one is the product of [4+3] cycloaddition of cyclopropane to a diene moiety of anthracene. The second one also has a seven-membered ring and is formed by the Lewis acid catalyzed electrophilic attack of cyclopropane onto the C9 atom of anthracene followed by intramolecular attack of the formed arenonium ion on aryl group of the starting cyclopropane. Lastly, the common Friedel–Crafts products are formed. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Top-30
Citations by journals
|
2
4
6
8
10
|
|
|
Organic Letters
10 publications, 15.15%
|
|
|
Journal of Organic Chemistry
7 publications, 10.61%
|
|
|
Chemistry - A European Journal
6 publications, 9.09%
|
|
|
Organic and Biomolecular Chemistry
5 publications, 7.58%
|
|
|
European Journal of Organic Chemistry
4 publications, 6.06%
|
|
|
Angewandte Chemie - International Edition
4 publications, 6.06%
|
|
|
Angewandte Chemie
4 publications, 6.06%
|
|
|
Tetrahedron
3 publications, 4.55%
|
|
|
Journal of the American Chemical Society
3 publications, 4.55%
|
|
|
Chemical Communications
2 publications, 3.03%
|
|
|
Tetrahedron Letters
2 publications, 3.03%
|
|
|
Asian Journal of Organic Chemistry
2 publications, 3.03%
|
|
|
Synthesis
2 publications, 3.03%
|
|
|
Science China Chemistry
1 publication, 1.52%
|
|
|
ACS Catalysis
1 publication, 1.52%
|
|
|
Mendeleev Communications
1 publication, 1.52%
|
|
|
Israel Journal of Chemistry
1 publication, 1.52%
|
|
|
Chemical Record
1 publication, 1.52%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 1.52%
|
|
|
Organometallics
1 publication, 1.52%
|
|
|
Chemical Science
1 publication, 1.52%
|
|
|
RSC Advances
1 publication, 1.52%
|
|
|
Russian Chemical Reviews
1 publication, 1.52%
|
|
|
2
4
6
8
10
|
Citations by publishers
|
5
10
15
20
25
|
|
|
Wiley
23 publications, 34.85%
|
|
|
American Chemical Society (ACS)
22 publications, 33.33%
|
|
|
Royal Society of Chemistry (RSC)
9 publications, 13.64%
|
|
|
Elsevier
7 publications, 10.61%
|
|
|
Thieme
2 publications, 3.03%
|
|
|
Springer Nature
1 publication, 1.52%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.52%
|
|
|
5
10
15
20
25
|
- 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":[2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[2,5,6,3,4,4,8,6,6,2,7,2,5,2,2,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["3.03","7.58","9.09","4.55","6.06","6.06","12.12","9.09","9.09","3.03","10.61","3.03","7.58","3.03","3.03","3.03"],"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":["Organic Letters","Journal of Organic Chemistry","Chemistry - A European Journal","Organic and Biomolecular Chemistry","European Journal of Organic Chemistry","Angewandte Chemie - International Edition","Angewandte Chemie","Tetrahedron","Journal of the American Chemical Society","Chemical Communications","Tetrahedron Letters","Asian Journal of Organic Chemistry","Synthesis","Science China Chemistry","ACS Catalysis","Mendeleev Communications","Israel Journal of Chemistry","Chemical Record","Advanced Synthesis and Catalysis","Organometallics","Chemical Science","RSC Advances","Russian Chemical Reviews"],"ids":[3315,8697,24708,541,19472,19215,25450,3439,4813,9073,6133,9409,10934,14409,4873,5294,17699,22413,3906,1409,9646,3100,23802],"codes":[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\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[10,7,6,5,4,4,4,3,3,2,2,2,2,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[15.15,10.61,9.09,7.58,6.06,6.06,6.06,4.55,4.55,3.03,3.03,3.03,3.03,1.52,1.52,1.52,1.52,1.52,1.52,1.52,1.52,1.52,1.52],"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":["Wiley","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Elsevier","Thieme","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,135,8,9422],"codes":[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\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[23,22,9,7,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[34.85,33.33,13.64,10.61,3.03,1.52,1.52],"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":[2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,2,0,0,0,0,0,0,0,1,0,0,0,0,0],"percentage":["0","0","3.03","0","0","0","0","0","0","0","1.52","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[1,0,1,0,0,1,1,1,2,0,1,1,1,0,0,0],"percentage":["1.52","0","1.52","0","0","1.52","1.52","1.52","3.03","0","1.52","1.52","1.52","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,5,3,3,4,2,6,5,4,2,5,1,4,2,2,2],"percentage":["1.52","7.58","4.55","4.55","6.06","3.03","9.09","7.58","6.06","3.03","7.58","1.52","6.06","3.03","3.03","3.03"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,0,0,0,1,1,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","1.52","1.52","0","0","0","0","0","0","0","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":[2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[1,0,2,0,0,1,0,1,0,0,1,0,0,0,0,0],"percentage":["1.52","0","3.03","0","0","1.52","0","1.52","0","0","1.52","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,2,2,0,3,3,3,1,1,1,4,1,1,1],"percentage":["0","0","1.52","3.03","3.03","0","4.55","4.55","4.55","1.52","1.52","1.52","6.06","1.52","1.52","1.52"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,4,3,1,2,1,4,2,2,1,4,1,1,1,1,1],"percentage":["1.52","6.06","4.55","1.52","3.03","1.52","6.06","3.03","3.03","1.52","6.06","1.52","1.52","1.52","1.52","1.52"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,1,0,0,0,2,1,0,1,0,1,0,0,0,0,0],"percentage":["0","1.52","0","0","0","3.03","1.52","0","1.52","0","1.52","0","0","0","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
Ivanova O. et al. Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes // European Journal of Organic Chemistry. 2008. Vol. 2008. No. 31. pp. 5329-5335.
GOST all authors (up to 50)
Copy
Ivanova O., Budynina E. M., Grishin Y., Trushkov I. V., Verteletskii P. V. Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes // European Journal of Organic Chemistry. 2008. Vol. 2008. No. 31. pp. 5329-5335.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/ejoc.200800620
UR - https://doi.org/10.1002/ejoc.200800620
TI - Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes
T2 - European Journal of Organic Chemistry
AU - Ivanova, Olga
AU - Budynina, Ekaterina M
AU - Grishin, Yuri
AU - Trushkov, Igor V
AU - Verteletskii, Pavel V
PY - 2008
DA - 2008/11/01 00:00:00
PB - Wiley
SP - 5329-5335
IS - 31
VL - 2008
SN - 1434-193X
SN - 1099-0690
ER -
Cite this
BibTex
Copy
@article{2008_Ivanova,
author = {Olga Ivanova and Ekaterina M Budynina and Yuri Grishin and Igor V Trushkov and Pavel V Verteletskii},
title = {Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes},
journal = {European Journal of Organic Chemistry},
year = {2008},
volume = {2008},
publisher = {Wiley},
month = {nov},
url = {https://doi.org/10.1002/ejoc.200800620},
number = {31},
pages = {5329--5335},
doi = {10.1002/ejoc.200800620}
}
Cite this
MLA
Copy
Ivanova, Olga, et al. “Lewis Acid Catalyzed Reactions of Donor-Acceptor Cyclopropanes with Anthracenes.” European Journal of Organic Chemistry, vol. 2008, no. 31, Nov. 2008, pp. 5329-5335. https://doi.org/10.1002/ejoc.200800620.