Tetrahedron Letters, volume 49, issue 15, pages 2359-2362
An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones
Publication type: Journal Article
Publication date: 2008-04-01
Journal:
Tetrahedron Letters
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.8
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
The electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones offers an efficient and straightforward route to highly substituted furans under extremely mild reaction conditions. Iodine, NIS, and PhSeBr have proven successful as electrophiles in this process.
Top-30
Citations by journals
2
4
6
8
10
|
|
Journal of Organic Chemistry
10 publications, 19.61%
|
|
European Journal of Organic Chemistry
6 publications, 11.76%
|
|
Organic Letters
5 publications, 9.8%
|
|
Chemical Communications
5 publications, 9.8%
|
|
Russian Chemical Bulletin
2 publications, 3.92%
|
|
Tetrahedron Letters
2 publications, 3.92%
|
|
Journal of Fluorine Chemistry
2 publications, 3.92%
|
|
Chemistry - A European Journal
2 publications, 3.92%
|
|
Organic and Biomolecular Chemistry
2 publications, 3.92%
|
|
Synthesis
2 publications, 3.92%
|
|
Chemical and Pharmaceutical Bulletin
1 publication, 1.96%
|
|
Bulletin of the Korean Chemical Society
1 publication, 1.96%
|
|
Tetrahedron
1 publication, 1.96%
|
|
ChemInform
1 publication, 1.96%
|
|
Applied Organometallic Chemistry
1 publication, 1.96%
|
|
Advanced Synthesis and Catalysis
1 publication, 1.96%
|
|
Chemical Reviews
1 publication, 1.96%
|
|
Topics in Heterocyclic Chemistry
1 publication, 1.96%
|
|
Progress in Heterocyclic Chemistry
1 publication, 1.96%
|
|
Organic Reaction Mechanisms
1 publication, 1.96%
|
|
Russian Chemical Reviews
1 publication, 1.96%
|
|
2
4
6
8
10
|
Citations by publishers
2
4
6
8
10
12
14
16
|
|
American Chemical Society (ACS)
16 publications, 31.37%
|
|
Wiley
13 publications, 25.49%
|
|
Elsevier
7 publications, 13.73%
|
|
Royal Society of Chemistry (RSC)
7 publications, 13.73%
|
|
Springer Nature
3 publications, 5.88%
|
|
Thieme
2 publications, 3.92%
|
|
Pharmaceutical Society of Japan
1 publication, 1.96%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.96%
|
|
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":[2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[2,8,6,9,6,2,6,1,2,1,0,1,1,2,1,1,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["3.92","15.69","11.76","17.65","11.76","3.92","11.76","1.96","3.92","1.96",0,"1.96","1.96","3.92","1.96","1.96","3.92"],"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","European Journal of Organic Chemistry","Organic Letters","Chemical Communications","Russian Chemical Bulletin","Tetrahedron Letters","Journal of Fluorine Chemistry","Chemistry - A European Journal","Organic and Biomolecular Chemistry","Synthesis","Chemical and Pharmaceutical Bulletin","Bulletin of the Korean Chemical Society","Tetrahedron","ChemInform","Applied Organometallic Chemistry","Advanced Synthesis and Catalysis","Chemical Reviews","Topics in Heterocyclic Chemistry","Progress in Heterocyclic Chemistry","Organic Reaction Mechanisms","Russian Chemical Reviews"],"ids":[8697,19472,3315,9073,10918,6133,14755,24708,541,10934,20999,7473,3439,25372,11683,3906,13718,38323,17224,42256,23802],"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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/KBGMujzjwr0rGFxg8Kz0qvYdFHkcBo5w0GTtfiiU_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_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\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[10,6,5,5,2,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[19.61,11.76,9.8,9.8,3.92,3.92,3.92,3.92,3.92,3.92,1.96,1.96,1.96,1.96,1.96,1.96,1.96,1.96,1.96,1.96,1.96],"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":["American Chemical Society (ACS)","Wiley","Elsevier","Royal Society of Chemistry (RSC)","Springer Nature","Thieme","Pharmaceutical Society of Japan","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[40,11,17,123,8,135,159,9422],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/KBGMujzjwr0rGFxg8Kz0qvYdFHkcBo5w0GTtfiiU_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[16,13,7,7,3,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[31.37,25.49,13.73,13.73,5.88,3.92,1.96,1.96],"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":[2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,0,1,2,0,1,0,0,0,0,0,0,1,0,0,1],"percentage":["0","1.96","0","1.96","3.92","0","1.96","0","0","0","0","0","0","1.96","0","0","1.96"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,1,2,0,2,0,2,0,2,0,0,0,0,0,0,0,0],"percentage":["0","1.96","3.92","0","3.92","0","3.92","0","3.92","0","0","0","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,5,4,6,2,2,2,1,0,1,0,1,1,1,1,0,1],"percentage":["1.96","9.8","7.84","11.76","3.92","3.92","3.92","1.96","0","1.96","0","1.96","1.96","1.96","1.96","0","1.96"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,1,0,2,0,0,1,0,0,0,0,0,0,0,0,1,0],"percentage":["1.96","1.96","0","3.92","0","0","1.96","0","0","0","0","0","0","0","0","1.96","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":[2008,2009,2010,2011,2012,2013,2014,2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[],"codes":[],"imageUrls":[],"datasets":[{"label":"Q4","backgroundColor":"rgb(221,90,78)","data":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,1,1,3,0,1,0,0,0,0,0,0,1,0,0,1],"percentage":["0","1.96","1.96","1.96","5.88","0","1.96","0","0","0","0","0","0","1.96","0","0","1.96"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,4,0,2,2,0,3,1,2,1,0,1,1,0,0,0,0],"percentage":["0","7.84","0","3.92","3.92","0","5.88","1.96","3.92","1.96","0","1.96","1.96","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,2,5,4,1,2,1,0,0,0,0,0,0,1,1,0,1],"percentage":["1.96","3.92","9.8","7.84","1.96","3.92","1.96","0","0","0","0","0","0","1.96","1.96","0","1.96"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,1,0,2,0,0,1,0,0,0,0,0,0,0,0,1,0],"percentage":["1.96","1.96","0","3.92","0","0","1.96","0","0","0","0","0","0","0","0","1.96","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
Huang X. et al. An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones // Tetrahedron Letters. 2008. Vol. 49. No. 15. pp. 2359-2362.
GOST all authors (up to 50)
Copy
Huang X., Fu W., Miao M. An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones // Tetrahedron Letters. 2008. Vol. 49. No. 15. pp. 2359-2362.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.tetlet.2008.02.081
UR - https://doi.org/10.1016/j.tetlet.2008.02.081
TI - An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones
T2 - Tetrahedron Letters
AU - Huang, Xian
AU - Fu, Wei-jun
AU - Miao, Maozhong
PY - 2008
DA - 2008/04/01 00:00:00
PB - Elsevier
SP - 2359-2362
IS - 15
VL - 49
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex
Copy
@article{2008_Huang,
author = {Xian Huang and Wei-jun Fu and Maozhong Miao},
title = {An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones},
journal = {Tetrahedron Letters},
year = {2008},
volume = {49},
publisher = {Elsevier},
month = {apr},
url = {https://doi.org/10.1016/j.tetlet.2008.02.081},
number = {15},
pages = {2359--2362},
doi = {10.1016/j.tetlet.2008.02.081}
}
Cite this
MLA
Copy
Huang, Xian, et al. “An efficient synthesis of highly substituted furans via the electrophilic cyclization of 1-(1-alkynyl)-cyclopropyl ketones.” Tetrahedron Letters, vol. 49, no. 15, Apr. 2008, pp. 2359-2362. https://doi.org/10.1016/j.tetlet.2008.02.081.