Organic and Biomolecular Chemistry, volume 13, issue 3, pages 655-671
Carbocycles from donor–acceptor cyclopropanes
1
The University of Western Ontario, Department of Chemistry, London, Ontario, Canada N6A 5B7
|
Publication type: Journal Article
Publication date: 2015-01-01
Journal:
Organic and Biomolecular Chemistry
Quartile SCImago
Q1
Quartile WOS
Q2
Impact factor: 3.2
ISSN: 14770520, 14770539
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Donor–acceptor cyclopropane annulations – not just for heterocycles.
Top-30
Citations by journals
|
10
20
30
40
50
60
70
|
|
|
Organic Letters
66 publications, 14.83%
|
|
|
Journal of Organic Chemistry
44 publications, 9.89%
|
|
|
European Journal of Organic Chemistry
31 publications, 6.97%
|
|
|
Angewandte Chemie - International Edition
30 publications, 6.74%
|
|
|
Angewandte Chemie
30 publications, 6.74%
|
|
|
Organic and Biomolecular Chemistry
21 publications, 4.72%
|
|
|
Advanced Synthesis and Catalysis
21 publications, 4.72%
|
|
|
Chemistry - A European Journal
19 publications, 4.27%
|
|
|
Chemical Communications
17 publications, 3.82%
|
|
|
RSC Advances
12 publications, 2.7%
|
|
|
Synthesis
10 publications, 2.25%
|
|
|
Organic Chemistry Frontiers
9 publications, 2.02%
|
|
|
Tetrahedron Letters
9 publications, 2.02%
|
|
|
ACS Catalysis
9 publications, 2.02%
|
|
|
Israel Journal of Chemistry
8 publications, 1.8%
|
|
|
Journal of the American Chemical Society
6 publications, 1.35%
|
|
|
ChemistrySelect
6 publications, 1.35%
|
|
|
Chemical Reviews
6 publications, 1.35%
|
|
|
Russian Chemical Bulletin
5 publications, 1.12%
|
|
|
Asian Journal of Organic Chemistry
5 publications, 1.12%
|
|
|
Synlett
5 publications, 1.12%
|
|
|
Molecules
3 publications, 0.67%
|
|
|
Beilstein Journal of Organic Chemistry
3 publications, 0.67%
|
|
|
Nature Communications
3 publications, 0.67%
|
|
|
Accounts of Chemical Research
3 publications, 0.67%
|
|
|
Chemical Science
3 publications, 0.67%
|
|
|
Bulletin of the Chemical Society of Japan
2 publications, 0.45%
|
|
|
Frontiers in Chemistry
2 publications, 0.45%
|
|
|
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
2 publications, 0.45%
|
|
|
10
20
30
40
50
60
70
|
Citations by publishers
|
20
40
60
80
100
120
140
160
180
|
|
|
Wiley
164 publications, 36.85%
|
|
|
American Chemical Society (ACS)
138 publications, 31.01%
|
|
|
Royal Society of Chemistry (RSC)
66 publications, 14.83%
|
|
|
Elsevier
22 publications, 4.94%
|
|
|
Thieme
15 publications, 3.37%
|
|
|
Springer Nature
10 publications, 2.25%
|
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
6 publications, 1.35%
|
|
|
Beilstein-Institut
3 publications, 0.67%
|
|
|
The Chemical Society of Japan
3 publications, 0.67%
|
|
|
Pharmaceutical Society of Japan
2 publications, 0.45%
|
|
|
Shanghai Institute of Organic Chemistry
2 publications, 0.45%
|
|
|
Frontiers Media S.A.
2 publications, 0.45%
|
|
|
Society of Synthetic Organic Chemistry
2 publications, 0.45%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 0.45%
|
|
|
Bentham Science
1 publication, 0.22%
|
|
|
SAGE
1 publication, 0.22%
|
|
|
Korean Chemical Society
1 publication, 0.22%
|
|
|
Walter de Gruyter
1 publication, 0.22%
|
|
|
Pleiades Publishing
1 publication, 0.22%
|
|
|
American Institute of Physics (AIP)
1 publication, 0.22%
|
|
|
The Japan Institute of Heterocyclic Chemistry
1 publication, 0.22%
|
|
|
20
40
60
80
100
120
140
160
180
|
- 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":[2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[32,55,60,48,53,46,46,38,36,31],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["7.19","12.36","13.48","10.79","11.91","10.34","10.34","8.54","8.09","6.97"],"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","European Journal of Organic Chemistry","Angewandte Chemie - International Edition","Angewandte Chemie","Organic and Biomolecular Chemistry","Advanced Synthesis and Catalysis","Chemistry - A European Journal","Chemical Communications","RSC Advances","Synthesis","Organic Chemistry Frontiers","Tetrahedron Letters","ACS Catalysis","Israel Journal of Chemistry","Journal of the American Chemical Society","ChemistrySelect","Chemical Reviews","Russian Chemical Bulletin","Asian Journal of Organic Chemistry","Synlett","Molecules","Beilstein Journal of Organic Chemistry","Nature Communications","Accounts of Chemical Research","Chemical Science","Bulletin of the Chemical Society of Japan","Frontiers in Chemistry","Yuki Gosei Kagaku Kyokaishi\/Journal of Synthetic Organic Chemistry"],"ids":[3315,8697,19472,19215,25450,541,3906,24708,9073,3100,10934,3991,6133,4873,17699,4813,8021,13718,10918,9409,10217,1770,21928,3231,1526,9646,20870,6407,3551],"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\/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\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ktSZPrGjOMvauY6mn7jk8bqo3Af0S6abv653w90B_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/QzzkQMUwda0fYU3txrAv3z24JfXJEjptEQpWMERc_medium.webp"],"datasets":[{"label":"","data":[66,44,31,30,30,21,21,19,17,12,10,9,9,9,8,6,6,6,5,5,5,3,3,3,3,3,2,2,2],"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":[14.83,9.89,6.97,6.74,6.74,4.72,4.72,4.27,3.82,2.7,2.25,2.02,2.02,2.02,1.8,1.35,1.35,1.35,1.12,1.12,1.12,0.67,0.67,0.67,0.67,0.67,0.45,0.45,0.45],"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","Multidisciplinary Digital Publishing Institute (MDPI)","Beilstein-Institut","The Chemical Society of Japan","Pharmaceutical Society of Japan","Shanghai Institute of Organic Chemistry","Frontiers Media S.A.","Society of Synthetic Organic Chemistry","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Bentham Science","SAGE","Korean Chemical Society","Walter de Gruyter","Pleiades Publishing","American Institute of Physics (AIP)","The Japan Institute of Heterocyclic Chemistry"],"ids":[11,40,123,17,135,8,202,6139,6950,159,8960,208,1303,9422,39,31,6493,4,101,250,9411],"codes":[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\/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\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/ktSZPrGjOMvauY6mn7jk8bqo3Af0S6abv653w90B_medium.webp","\/storage\/images\/resized\/KBGMujzjwr0rGFxg8Kz0qvYdFHkcBo5w0GTtfiiU_medium.webp","\/storage\/images\/resized\/6EJSsoiR4fNMNMPFBpMh5yKuYKcPXJDQKvKVeEMy_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","\/storage\/images\/resized\/QzzkQMUwda0fYU3txrAv3z24JfXJEjptEQpWMERc_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/ruydfaB80LDjlkYqsfOeUAZohOIODyq7bQzis5O7_medium.webp","\/storage\/images\/resized\/IYy5KbQWZ2uxYLvcvjXjlXRDR3xNOFyFK4Kl6043_medium.webp","\/storage\/images\/resized\/3SpVxcYL33bOvPq4sHxJLH2NeKNeDloahSUpNiO4_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp","\/storage\/images\/resized\/ARM4e6URKRsbRZvIF0vFis9DjxGloBjnBYJXbHmZ_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp"],"datasets":[{"label":"","data":[164,138,66,22,15,10,6,3,3,2,2,2,2,2,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[36.85,31.01,14.83,4.94,3.37,2.25,1.35,0.67,0.67,0.45,0.45,0.45,0.45,0.45,0.22,0.22,0.22,0.22,0.22,0.22,0.22],"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":[2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,1,1,0,0,1,2,0,0,1],"percentage":["0","0.22","0.22","0","0","0.22","0.45","0","0","0.22"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[2,2,3,2,4,2,2,2,3,4],"percentage":["0.45","0.45","0.67","0.45","0.9","0.45","0.45","0.45","0.67","0.9"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[6,7,8,3,13,9,8,6,9,5],"percentage":["1.35","1.57","1.8","0.67","2.92","2.02","1.8","1.35","2.02","1.12"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[23,45,48,43,35,33,34,28,23,20],"percentage":["5.17","10.11","10.79","9.66","7.87","7.42","7.64","6.29","5.17","4.49"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,1,1,0,2,1,1],"percentage":["0.22","0","0","0","0.22","0.22","0","0.45","0.22","0.22"]}]},"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":[2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[1,0,2,0,1,1,2,0,0,0],"percentage":["0.22","0","0.45","0","0.22","0.22","0.45","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[3,5,3,3,4,5,3,4,6,3],"percentage":["0.67","1.12","0.67","0.67","0.9","1.12","0.67","0.9","1.35","0.67"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[9,21,17,7,25,11,17,15,15,12],"percentage":["2.02","4.72","3.82","1.57","5.62","2.47","3.82","3.37","3.37","2.7"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[15,25,32,32,19,27,20,15,12,13],"percentage":["3.37","5.62","7.19","7.19","4.27","6.07","4.49","3.37","2.7","2.92"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[4,4,6,6,4,2,4,4,3,3],"percentage":["0.9","0.9","1.35","1.35","0.9","0.45","0.9","0.9","0.67","0.67"]}]},"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
Grover H. K., Emmett M. R., Kerr M. A. Carbocycles from donor–acceptor cyclopropanes // Organic and Biomolecular Chemistry. 2015. Vol. 13. No. 3. pp. 655-671.
GOST all authors (up to 50)
Copy
Grover H. K., Emmett M. R., Kerr M. A. Carbocycles from donor–acceptor cyclopropanes // Organic and Biomolecular Chemistry. 2015. Vol. 13. No. 3. pp. 655-671.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/C4OB02117G
UR - https://doi.org/10.1039/C4OB02117G
TI - Carbocycles from donor–acceptor cyclopropanes
T2 - Organic and Biomolecular Chemistry
AU - Grover, Huck K
AU - Emmett, Michael R
AU - Kerr, M A
PY - 2015
DA - 2015/01/01 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 655-671
IS - 3
VL - 13
SN - 1477-0520
SN - 1477-0539
ER -
Cite this
BibTex
Copy
@article{2015_Grover,
author = {Huck K Grover and Michael R Emmett and M A Kerr},
title = {Carbocycles from donor–acceptor cyclopropanes},
journal = {Organic and Biomolecular Chemistry},
year = {2015},
volume = {13},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/C4OB02117G},
number = {3},
pages = {655--671},
doi = {10.1039/C4OB02117G}
}
Cite this
MLA
Copy
Grover, Huck K., et al. “Carbocycles from donor–acceptor cyclopropanes.” Organic and Biomolecular Chemistry, vol. 13, no. 3, Jan. 2015, pp. 655-671. https://doi.org/10.1039/C4OB02117G.