Organic and Biomolecular Chemistry, volume 18, issue 36, pages 7127-7138
Cu(i )-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs)
Publication type: Journal Article
Publication date: 2020-08-26
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
A novel synthesis of 3-trifluoroethylcyclopenta[
Top-30
Citations by journals
1
2
|
|
Advanced Synthesis and Catalysis
2 publications, 22.22%
|
|
Molecules
1 publication, 11.11%
|
|
Journal of Organic Chemistry
1 publication, 11.11%
|
|
Chemical Science
1 publication, 11.11%
|
|
Organic Chemistry Frontiers
1 publication, 11.11%
|
|
European Journal of Organic Chemistry
1 publication, 11.11%
|
|
Russian Chemical Reviews
1 publication, 11.11%
|
|
Organic Reaction Mechanisms
1 publication, 11.11%
|
|
1
2
|
Citations by publishers
1
2
3
4
|
|
Wiley
4 publications, 44.44%
|
|
Royal Society of Chemistry (RSC)
2 publications, 22.22%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 11.11%
|
|
American Chemical Society (ACS)
1 publication, 11.11%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 11.11%
|
|
1
2
3
4
|
- 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":[2020,2021,2022,2023,2024],"ids":[0,0,0,0,0],"codes":[0,0,0,0,0],"imageUrls":["","","","",""],"datasets":[{"label":"Citations number","data":[1,0,5,1,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["11.11",0,"55.56","11.11","22.22"],"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":["Advanced Synthesis and Catalysis","Molecules","Journal of Organic Chemistry","Chemical Science","Organic Chemistry Frontiers","European Journal of Organic Chemistry","Russian Chemical Reviews","Organic Reaction Mechanisms"],"ids":[3906,1770,8697,9646,3991,19472,23802,42256],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp"],"datasets":[{"label":"","data":[2,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[22.22,11.11,11.11,11.11,11.11,11.11,11.11,11.11],"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","Royal Society of Chemistry (RSC)","Multidisciplinary Digital Publishing Institute (MDPI)","American Chemical Society (ACS)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,123,202,40,9422],"codes":[0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[4,2,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[44.44,22.22,11.11,11.11,11.11],"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":[2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0],"percentage":["0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0],"percentage":["0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,0,0],"percentage":["0","0","11.11","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,0,4,1,1],"percentage":["11.11","0","44.44","11.11","11.11"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,0,0,1],"percentage":["0","0","0","0","11.11"]}]},"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":[2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0],"percentage":["0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0],"percentage":["0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,1,0],"percentage":["0","0","11.11","11.11","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,0,4,0,1],"percentage":["11.11","0","44.44","0","11.11"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,0,0,1],"percentage":["0","0","0","0","11.11"]}]},"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
Li P. H. et al. Cu(i)-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs) // Organic and Biomolecular Chemistry. 2020. Vol. 18. No. 36. pp. 7127-7138.
GOST all authors (up to 50)
Copy
Li P. H., Li P., Wei Yin 尹., Shi M. Cu(i)-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs) // Organic and Biomolecular Chemistry. 2020. Vol. 18. No. 36. pp. 7127-7138.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/d0ob01692f
UR - https://doi.org/10.1039/d0ob01692f
TI - Cu(i)-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs)
T2 - Organic and Biomolecular Chemistry
AU - Li, Peng Hua
AU - Shi, Min
AU - Wei Yin, 尹维
AU - Li, Peng-hua
PY - 2020
DA - 2020/08/26 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 7127-7138
IS - 36
VL - 18
SN - 1477-0520
SN - 1477-0539
ER -
Cite this
BibTex
Copy
@article{2020_Li,
author = {Peng Hua Li and Min Shi and 尹维 Wei Yin and Peng-hua Li},
title = {Cu(i)-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs)},
journal = {Organic and Biomolecular Chemistry},
year = {2020},
volume = {18},
publisher = {Royal Society of Chemistry (RSC)},
month = {aug},
url = {https://doi.org/10.1039/d0ob01692f},
number = {36},
pages = {7127--7138},
doi = {10.1039/d0ob01692f}
}
Cite this
MLA
Copy
Li, Peng Hua, et al. “Cu(i)-Catalyzed addition–cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs).” Organic and Biomolecular Chemistry, vol. 18, no. 36, Aug. 2020, pp. 7127-7138. https://doi.org/10.1039/d0ob01692f.