Organic Letters, volume 14, issue 13, pages 3430-3433
A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane
Publication type: Journal Article
Publication date: 2012-06-12
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
A silver(I)-catalyzed tandem reaction of 2-alkynylbenzaldoxime with alkylidenecyclopropane gives rise to benzo-7-azabicyclo[4.2.2]dec-7-en-4-ones in moderate to good yields. The complexity and diversity could be easily incorporated with the formation of three bonds during the process.
Top-30
Citations by journals
|
1
2
3
4
5
6
7
8
|
|
|
Tetrahedron
8 publications, 16.67%
|
|
|
Organic and Biomolecular Chemistry
6 publications, 12.5%
|
|
|
Organic Letters
5 publications, 10.42%
|
|
|
Advanced Synthesis and Catalysis
3 publications, 6.25%
|
|
|
Organic Chemistry Frontiers
3 publications, 6.25%
|
|
|
European Journal of Organic Chemistry
2 publications, 4.17%
|
|
|
Chemistry - A European Journal
2 publications, 4.17%
|
|
|
Journal of Organic Chemistry
2 publications, 4.17%
|
|
|
Chemical Reviews
2 publications, 4.17%
|
|
|
Chemical Communications
2 publications, 4.17%
|
|
|
Russian Chemical Bulletin
1 publication, 2.08%
|
|
|
Journal of the Iranian Chemical Society
1 publication, 2.08%
|
|
|
Tetrahedron Letters
1 publication, 2.08%
|
|
|
Israel Journal of Chemistry
1 publication, 2.08%
|
|
|
ChemistrySelect
1 publication, 2.08%
|
|
|
Chemistry - An Asian Journal
1 publication, 2.08%
|
|
|
ChemInform
1 publication, 2.08%
|
|
|
RSC Advances
1 publication, 2.08%
|
|
|
Chemical Society Reviews
1 publication, 2.08%
|
|
|
Heterocycles
1 publication, 2.08%
|
|
|
Russian Chemical Reviews
1 publication, 2.08%
|
|
|
1
2
3
4
5
6
7
8
|
Citations by publishers
|
2
4
6
8
10
12
14
|
|
|
Wiley
13 publications, 27.08%
|
|
|
Royal Society of Chemistry (RSC)
13 publications, 27.08%
|
|
|
Elsevier
9 publications, 18.75%
|
|
|
American Chemical Society (ACS)
9 publications, 18.75%
|
|
|
Springer Nature
2 publications, 4.17%
|
|
|
The Japan Institute of Heterocyclic Chemistry
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
|
- 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":[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],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,8,16,3,5,2,3,3,0,2,3,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["2.08","16.67","33.33","6.25","10.42","4.17","6.25","6.25",0,"4.17","6.25","2.08","2.08"],"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":["Tetrahedron","Organic and Biomolecular Chemistry","Organic Letters","Advanced Synthesis and Catalysis","Organic Chemistry Frontiers","European Journal of Organic Chemistry","Chemistry - A European Journal","Journal of Organic Chemistry","Chemical Reviews","Chemical Communications","Russian Chemical Bulletin","Journal of the Iranian Chemical Society","Tetrahedron Letters","Israel Journal of Chemistry","ChemistrySelect","Chemistry - An Asian Journal","ChemInform","RSC Advances","Chemical Society Reviews","Heterocycles","Russian Chemical Reviews"],"ids":[3439,541,3315,3906,3991,19472,24708,8697,13718,9073,10918,15384,6133,17699,8021,10120,25372,3100,20586,22287,23802],"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\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_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\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[8,6,5,3,3,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[16.67,12.5,10.42,6.25,6.25,4.17,4.17,4.17,4.17,4.17,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08,2.08],"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":["Wiley","Royal Society of Chemistry (RSC)","Elsevier","American Chemical Society (ACS)","Springer Nature","The Japan Institute of Heterocyclic Chemistry","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,123,17,40,8,9411,9422],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/SovkqI6gX6to8o5XBnS9RNxEOYVicn7hatkMzrvl_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[13,13,9,9,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[27.08,27.08,18.75,18.75,4.17,2.08,2.08],"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":[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":[0,0,1,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","2.08","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,0,0,0,1,0,0,0,0,1,0,0],"percentage":["0","2.08","0","0","0","2.08","0","0","0","0","2.08","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,4,5,0,1,0,0,1,0,0,0,1,0],"percentage":["0","8.33","10.42","0","2.08","0","0","2.08","0","0","0","2.08","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,3,10,3,4,1,1,2,0,2,2,0,1],"percentage":["0","6.25","20.83","6.25","8.33","2.08","2.08","4.17","0","4.17","4.17","0","2.08"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,2,0,0,0,0,0,0],"percentage":["2.08","0","0","0","0","0","4.17","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":[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":[0,0,1,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","2.08","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,3,5,0,0,1,0,1,0,0,1,1,0],"percentage":["0","6.25","10.42","0","0","2.08","0","2.08","0","0","2.08","2.08","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,4,5,1,2,0,0,0,0,1,2,0,0],"percentage":["0","8.33","10.42","2.08","4.17","0","0","0","0","2.08","4.17","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,1,5,2,3,1,1,2,0,1,0,0,1],"percentage":["0","2.08","10.42","4.17","6.25","2.08","2.08","4.17","0","2.08","0","0","2.08"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,2,0,0,0,0,0,0],"percentage":["2.08","0","0","0","0","0","4.17","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
Xiao Q., Ye S., Wu J. A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane // Organic Letters. 2012. Vol. 14. No. 13. pp. 3430-3433.
GOST all authors (up to 50)
Copy
Xiao Q., Ye S., Wu J. A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane // Organic Letters. 2012. Vol. 14. No. 13. pp. 3430-3433.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol301393f
UR - https://doi.org/10.1021/ol301393f
TI - A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane
T2 - Organic Letters
AU - Xiao, Qian
AU - Ye, Shengqing
AU - Wu, Jie
PY - 2012
DA - 2012/06/12 00:00:00
PB - American Chemical Society (ACS)
SP - 3430-3433
IS - 13
VL - 14
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex
Copy
@article{2012_Xiao,
author = {Qian Xiao and Shengqing Ye and Jie Wu},
title = {A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane},
journal = {Organic Letters},
year = {2012},
volume = {14},
publisher = {American Chemical Society (ACS)},
month = {jun},
url = {https://doi.org/10.1021/ol301393f},
number = {13},
pages = {3430--3433},
doi = {10.1021/ol301393f}
}
Cite this
MLA
Copy
Xiao, Qian, et al. “A Silver(I)-Catalyzed Tandem Reaction of 2-Alkynylbenzaldoxime with Alkylidenecyclopropane.” Organic Letters, vol. 14, no. 13, Jun. 2012, pp. 3430-3433. https://doi.org/10.1021/ol301393f.