Synlett, volume 26, issue 12, pages 1687-1692
Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles
Publication type: Journal Article
Publication date: 2015-05-04
Organic Chemistry
Abstract
A Sc(OTf)3-catalyzed cascade reaction consisting of a Friedel–Crafts alkylation followed by a Michael addition between cyclopropane 1,1-diesters and β-(indol-2-yl)-α,β-unsaturated ketones allows for the efficient synthesis of polysubstituted tetrahydrocarbazoles under very mild reaction conditions.
Top-30
Citations by journals
1
2
|
|
European Journal of Organic Chemistry
2 publications, 18.18%
|
|
Organic Letters
2 publications, 18.18%
|
|
Organic and Biomolecular Chemistry
2 publications, 18.18%
|
|
ChemInform
1 publication, 9.09%
|
|
Asian Journal of Organic Chemistry
1 publication, 9.09%
|
|
Journal of Organic Chemistry
1 publication, 9.09%
|
|
Organic Chemistry Frontiers
1 publication, 9.09%
|
|
Russian Chemical Reviews
1 publication, 9.09%
|
|
1
2
|
Citations by publishers
1
2
3
4
|
|
Wiley
4 publications, 36.36%
|
|
American Chemical Society (ACS)
3 publications, 27.27%
|
|
Royal Society of Chemistry (RSC)
3 publications, 27.27%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 9.09%
|
|
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":[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":[1,1,2,1,3,0,2,0,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["9.09","9.09","18.18","9.09","27.27",0,"18.18",0,0,"9.09"],"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":["European Journal of Organic Chemistry","Organic Letters","Organic and Biomolecular Chemistry","ChemInform","Asian Journal of Organic Chemistry","Journal of Organic Chemistry","Organic Chemistry Frontiers","Russian Chemical Reviews"],"ids":[19472,3315,541,25372,9409,8697,3991,23802],"codes":[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\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[2,2,2,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[18.18,18.18,18.18,9.09,9.09,9.09,9.09,9.09],"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)","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,9422],"codes":[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\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[4,3,3,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[36.36,27.27,27.27,9.09],"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":[0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,1,1,0,0,0,0,0],"percentage":["0","0","9.09","9.09","9.09","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,1,0,2,0,2,0,0,1],"percentage":["0","9.09","9.09","0","18.18","0","18.18","0","0","9.09"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,0,0,0,0],"percentage":["9.09","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":[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],"percentage":["0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,1,2,0,1,0,0,0],"percentage":["0","0","9.09","9.09","18.18","0","9.09","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,1,0,1,0,1,0,0,1],"percentage":["0","9.09","9.09","0","9.09","0","9.09","0","0","9.09"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,0,0,0,0],"percentage":["9.09","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 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 W., Zhang H., Chen W. Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles // Synlett. 2015. Vol. 26. No. 12. pp. 1687-1692.
GOST all authors (up to 50)
Copy
Chen W., Zhang H., Chen W. Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles // Synlett. 2015. Vol. 26. No. 12. pp. 1687-1692.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1055/s-0034-1380617
UR - https://doi.org/10.1055/s-0034-1380617
TI - Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles
T2 - Synlett
AU - Chen, Wenhao
AU - Zhang, Huanhuan
AU - Chen, Wei
PY - 2015
DA - 2015/05/04 00:00:00
PB - Thieme
SP - 1687-1692
IS - 12
VL - 26
SN - 0936-5214
SN - 1437-2096
ER -
Cite this
BibTex
Copy
@article{2015_Chen,
author = {Wenhao Chen and Huanhuan Zhang and Wei Chen},
title = {Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles},
journal = {Synlett},
year = {2015},
volume = {26},
publisher = {Thieme},
month = {may},
url = {https://doi.org/10.1055/s-0034-1380617},
number = {12},
pages = {1687--1692},
doi = {10.1055/s-0034-1380617}
}
Cite this
MLA
Copy
Chen, Wenhao, et al. “Sc(OTf)3-Catalyzed [3+3] Annulation of Cyclopropane 1,1-Diesters with β-(Indol-2-yl)-α,β-unsaturated Ketones: Synthesis of Polysubstituted Tetrahydrocarbazoles.” Synlett, vol. 26, no. 12, May. 2015, pp. 1687-1692. https://doi.org/10.1055/s-0034-1380617.