Organic Chemistry Frontiers, volume 4, issue 1, pages 86-90
A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
Publication type: Journal Article
Publication date: 2017-01-01
Journal:
Organic Chemistry Frontiers
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.4
ISSN: 20524110, 20524129
Organic Chemistry
Abstract
Trifluoromethylthiolation of methylenecyclopropanes (MCPs) has been developed by using AgSCF3/Na2S2O8as a trifluoromethylthiolation source (SCF3) to give trifluoromethylthiolated 1,2-dihydronaphthalene derivatives in moderate to good yields.
Top-30
Citations by journals
|
1
2
3
4
5
6
7
|
|
|
Journal of Organic Chemistry
7 publications, 14.58%
|
|
|
Organic and Biomolecular Chemistry
7 publications, 14.58%
|
|
|
Advanced Synthesis and Catalysis
6 publications, 12.5%
|
|
|
Organic Letters
5 publications, 10.42%
|
|
|
Chemical Communications
4 publications, 8.33%
|
|
|
Asian Journal of Organic Chemistry
2 publications, 4.17%
|
|
|
Organic Chemistry Frontiers
2 publications, 4.17%
|
|
|
New Journal of Chemistry
2 publications, 4.17%
|
|
|
Beilstein Journal of Organic Chemistry
1 publication, 2.08%
|
|
|
Chinese Journal of Organic Chemistry
1 publication, 2.08%
|
|
|
Molecules
1 publication, 2.08%
|
|
|
Tetrahedron
1 publication, 2.08%
|
|
|
Journal of Fluorine Chemistry
1 publication, 2.08%
|
|
|
Chemistry - An Asian Journal
1 publication, 2.08%
|
|
|
Synlett
1 publication, 2.08%
|
|
|
Synthesis
1 publication, 2.08%
|
|
|
Russian Chemical Reviews
1 publication, 2.08%
|
|
|
1
2
3
4
5
6
7
|
Citations by publishers
|
2
4
6
8
10
12
14
16
|
|
|
Royal Society of Chemistry (RSC)
15 publications, 31.25%
|
|
|
Wiley
13 publications, 27.08%
|
|
|
American Chemical Society (ACS)
12 publications, 25%
|
|
|
Elsevier
2 publications, 4.17%
|
|
|
Thieme
2 publications, 4.17%
|
|
|
Beilstein-Institut
1 publication, 2.08%
|
|
|
Shanghai Institute of Organic Chemistry
1 publication, 2.08%
|
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
1 publication, 2.08%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.08%
|
|
|
2
4
6
8
10
12
14
16
|
- 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":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[3,5,10,9,7,6,6,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["6.25","10.42","20.83","18.75","14.58","12.5","12.5","4.17"],"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":["Journal of Organic Chemistry","Organic and Biomolecular Chemistry","Advanced Synthesis and Catalysis","Organic Letters","Chemical Communications","Asian Journal of Organic Chemistry","Organic Chemistry Frontiers","New Journal of Chemistry","Beilstein Journal of Organic Chemistry","Chinese Journal of Organic Chemistry","Molecules","Tetrahedron","Journal of Fluorine Chemistry","Chemistry - An Asian Journal","Synlett","Synthesis","Russian Chemical Reviews"],"ids":[8697,541,3906,3315,9073,9409,3991,1404,21928,11696,1770,3439,14755,10120,10217,10934,23802],"codes":[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\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/6EJSsoiR4fNMNMPFBpMh5yKuYKcPXJDQKvKVeEMy_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[7,7,6,5,4,2,2,2,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[14.58,14.58,12.5,10.42,8.33,4.17,4.17,4.17,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08],"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":["Royal Society of Chemistry (RSC)","Wiley","American Chemical Society (ACS)","Elsevier","Thieme","Beilstein-Institut","Shanghai Institute of Organic Chemistry","Multidisciplinary Digital Publishing Institute (MDPI)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[123,11,40,17,135,6139,8960,202,9422],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/6EJSsoiR4fNMNMPFBpMh5yKuYKcPXJDQKvKVeEMy_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[15,13,12,2,2,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[31.25,27.08,25,4.17,4.17,2.08,2.08,2.08,2.08],"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":[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],"percentage":["0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,1,1,0,0],"percentage":["0","0","0","0","2.08","2.08","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,1,3,0,0,1,2,0],"percentage":["0","2.08","6.25","0","0","2.08","4.17","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[3,3,7,8,4,4,4,2],"percentage":["6.25","6.25","14.58","16.67","8.33","8.33","8.33","4.17"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,1,0,1,2,0,0,0],"percentage":["0","2.08","0","2.08","4.17","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":[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],"percentage":["0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,1,0,1,2,0,0],"percentage":["0","0","2.08","0","2.08","4.17","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,2,3,5,2,3,3,1],"percentage":["0","4.17","6.25","10.42","4.17","6.25","6.25","2.08"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[3,2,6,3,2,1,3,1],"percentage":["6.25","4.17","12.5","6.25","4.17","2.08","6.25","2.08"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,1,0,1,2,0,0,0],"percentage":["0","2.08","0","2.08","4.17","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
Chen M. T. et al. A facile approach for the trifluoromethylthiolation of methylenecyclopropanes // Organic Chemistry Frontiers. 2017. Vol. 4. No. 1. pp. 86-90.
GOST all authors (up to 50)
Copy
Chen M. T., Chen M., Tang X., Shi M. A facile approach for the trifluoromethylthiolation of methylenecyclopropanes // Organic Chemistry Frontiers. 2017. Vol. 4. No. 1. pp. 86-90.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1039/c6qo00536e
UR - https://doi.org/10.1039/c6qo00536e
TI - A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
T2 - Organic Chemistry Frontiers
AU - Chen, Min Tao
AU - Tang, Xiang-Ying
AU - Shi, Min
AU - Chen, Min-Tao
PY - 2017
DA - 2017/01/01 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 86-90
IS - 1
VL - 4
SN - 2052-4110
SN - 2052-4129
ER -
Cite this
BibTex
Copy
@article{2017_Chen,
author = {Min Tao Chen and Xiang-Ying Tang and Min Shi and Min-Tao Chen},
title = {A facile approach for the trifluoromethylthiolation of methylenecyclopropanes},
journal = {Organic Chemistry Frontiers},
year = {2017},
volume = {4},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c6qo00536e},
number = {1},
pages = {86--90},
doi = {10.1039/c6qo00536e}
}
Cite this
MLA
Copy
Chen, Min Tao, et al. “A facile approach for the trifluoromethylthiolation of methylenecyclopropanes.” Organic Chemistry Frontiers, vol. 4, no. 1, Jan. 2017, pp. 86-90. https://doi.org/10.1039/c6qo00536e.