Organic Letters, volume 12, issue 11, pages 2606-2609
Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes
Publication type: Journal Article
Publication date: 2010-05-12
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Lewis acid catalyzed cycloaddition of methylenecyclopropanes (MCPs) with o-quinonemethide analogues, derived from the corresponding salicylaldehydes and CH(OEt)(3), produces the corresponding cycloadducts 3 in moderate to high yields at room temperature (20 degrees C). Moreover, the compounds 3 can be transformed to the indene derivatives 5 at high temperature. Plausible mechanisms have been proposed on the basis of control experiments.
Top-30
Citations by journals
|
1
2
3
4
5
|
|
|
Chemical Communications
5 publications, 17.24%
|
|
|
Organic Letters
4 publications, 13.79%
|
|
|
Tetrahedron
3 publications, 10.34%
|
|
|
European Journal of Organic Chemistry
2 publications, 6.9%
|
|
|
Journal of Organic Chemistry
2 publications, 6.9%
|
|
|
Journal of the Iranian Chemical Society
1 publication, 3.45%
|
|
|
Chemistry - A European Journal
1 publication, 3.45%
|
|
|
Asian Journal of Organic Chemistry
1 publication, 3.45%
|
|
|
Chemistry - An Asian Journal
1 publication, 3.45%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 3.45%
|
|
|
Chemical Reviews
1 publication, 3.45%
|
|
|
Organic and Biomolecular Chemistry
1 publication, 3.45%
|
|
|
RSC Advances
1 publication, 3.45%
|
|
|
Progress in Heterocyclic Chemistry
1 publication, 3.45%
|
|
|
Russian Chemical Reviews
1 publication, 3.45%
|
|
|
1
2
3
4
5
|
Citations by publishers
|
1
2
3
4
5
6
7
8
9
|
|
|
Wiley
9 publications, 31.03%
|
|
|
American Chemical Society (ACS)
7 publications, 24.14%
|
|
|
Royal Society of Chemistry (RSC)
7 publications, 24.14%
|
|
|
Elsevier
4 publications, 13.79%
|
|
|
Springer Nature
1 publication, 3.45%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 3.45%
|
|
|
1
2
3
4
5
6
7
8
9
|
- 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":[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],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[2,3,6,1,6,1,1,5,1,1,1,0,0,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["6.9","10.34","20.69","3.45","20.69","3.45","3.45","17.24","3.45","3.45","3.45",0,0,0,"3.45"],"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":["Chemical Communications","Organic Letters","Tetrahedron","European Journal of Organic Chemistry","Journal of Organic Chemistry","Journal of the Iranian Chemical Society","Chemistry - A European Journal","Asian Journal of Organic Chemistry","Chemistry - An Asian Journal","Advanced Synthesis and Catalysis","Chemical Reviews","Organic and Biomolecular Chemistry","RSC Advances","Progress in Heterocyclic Chemistry","Russian Chemical Reviews"],"ids":[9073,3315,3439,19472,8697,15384,24708,9409,10120,3906,13718,541,3100,17224,23802],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_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\/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\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[5,4,3,2,2,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[17.24,13.79,10.34,6.9,6.9,3.45,3.45,3.45,3.45,3.45,3.45,3.45,3.45,3.45,3.45],"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","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,8,9422],"codes":[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\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[9,7,7,4,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[31.03,24.14,24.14,13.79,3.45,3.45],"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":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"yearsCitationsQuartiles":{"type":"bar","data":{"show":true,"labels":[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],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,0,0,1,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","3.45","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[1,1,0,0,1,0,1,1,0,1,1,0,0,0,0],"percentage":["3.45","3.45","0","0","3.45","0","3.45","3.45","0","3.45","3.45","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,1,6,0,5,1,0,1,1,0,0,0,0,0,1],"percentage":["3.45","3.45","20.69","0","17.24","3.45","0","3.45","3.45","0","0","0","0","0","3.45"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,1,0,1,0,0,0,2,0,0,0,0,0,0,0],"percentage":["0","3.45","0","3.45","0","0","0","6.9","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":[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],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,0,0,1,0,0,2,0,0,0,0,0,0,0],"percentage":["0","3.45","0","0","3.45","0","0","6.9","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[1,0,4,0,3,0,1,1,0,1,1,0,0,0,0],"percentage":["3.45","0","13.79","0","10.34","0","3.45","3.45","0","3.45","3.45","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,1,2,0,2,1,0,0,1,0,0,0,0,0,1],"percentage":["3.45","3.45","6.9","0","6.9","3.45","0","0","3.45","0","0","0","0","0","3.45"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,1,0,1,0,0,0,2,0,0,0,0,0,0,0],"percentage":["0","3.45","0","3.45","0","0","0","6.9","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
Jiang M., Shi M. Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes // Organic Letters. 2010. Vol. 12. No. 11. pp. 2606-2609.
GOST all authors (up to 50)
Copy
Jiang M., Shi M. Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes // Organic Letters. 2010. Vol. 12. No. 11. pp. 2606-2609.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol100814a
UR - https://doi.org/10.1021/ol100814a
TI - Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes
T2 - Organic Letters
AU - Jiang, Min
AU - Shi, Min
PY - 2010
DA - 2010/05/12 00:00:00
PB - American Chemical Society (ACS)
SP - 2606-2609
IS - 11
VL - 12
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex
Copy
@article{2010_Jiang,
author = {Min Jiang and Min Shi},
title = {Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes},
journal = {Organic Letters},
year = {2010},
volume = {12},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/ol100814a},
number = {11},
pages = {2606--2609},
doi = {10.1021/ol100814a}
}
Cite this
MLA
Copy
Jiang, Min, and Min Shi. “Lewis Acid Catalyzed Cycloaddition of Methylenecyclopropanes with Salicylaldehydes.” Organic Letters, vol. 12, no. 11, May. 2010, pp. 2606-2609. https://doi.org/10.1021/ol100814a.