Angewandte Chemie - International Edition, volume 49, issue 10, pages 1830-1833
Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes
Shinichi SAITO
1
,
Kyotaro Maeda
1
,
Ryu Yamasaki
1
,
Takuya Kitamura
1
,
Minami Nakagawa
1
,
Korehito Kato
1
,
Isao Azumaya
2
,
Hyuma Masu
2
1
Department of Chemistry, Faculty of Science, Kagurazaka, Shinjuku, Tokyo, 162‐8601 (Japan), Fax: (+81) 3‐5261‐4631 http://www.rs.kagu.tus.ac.jp/sslab/
|
Publication type: Journal Article
Publication date: 2010-03-01
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 16.6
ISSN: 14337851, 15213773
General Chemistry
Catalysis
Top-30
Citations by journals
2
4
6
8
10
|
|
Advanced Synthesis and Catalysis
10 publications, 12.35%
|
|
Angewandte Chemie - International Edition
9 publications, 11.11%
|
|
Angewandte Chemie
9 publications, 11.11%
|
|
Organic Letters
8 publications, 9.88%
|
|
Chemical Science
4 publications, 4.94%
|
|
Chemistry - A European Journal
3 publications, 3.7%
|
|
ACS Catalysis
3 publications, 3.7%
|
|
Tetrahedron
2 publications, 2.47%
|
|
Tetrahedron Letters
2 publications, 2.47%
|
|
Journal of the American Chemical Society
2 publications, 2.47%
|
|
Chemical Reviews
2 publications, 2.47%
|
|
Chemical Communications
2 publications, 2.47%
|
|
Organic Chemistry Frontiers
2 publications, 2.47%
|
|
Organic and Biomolecular Chemistry
2 publications, 2.47%
|
|
Chemistry Letters
1 publication, 1.23%
|
|
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
1 publication, 1.23%
|
|
Asian Journal of Organic Chemistry
1 publication, 1.23%
|
|
ChemInform
1 publication, 1.23%
|
|
Chemistry - An Asian Journal
1 publication, 1.23%
|
|
Organometallics
1 publication, 1.23%
|
|
Journal of Organic Chemistry
1 publication, 1.23%
|
|
Synthetic Communications
1 publication, 1.23%
|
|
Topics in Current Chemistry
1 publication, 1.23%
|
|
Organic Reaction Mechanisms
1 publication, 1.23%
|
|
Advanced Science
1 publication, 1.23%
|
|
Russian Chemical Reviews
1 publication, 1.23%
|
|
2
4
6
8
10
|
Citations by publishers
5
10
15
20
25
30
35
40
45
|
|
Wiley
42 publications, 51.85%
|
|
American Chemical Society (ACS)
17 publications, 20.99%
|
|
Royal Society of Chemistry (RSC)
10 publications, 12.35%
|
|
Elsevier
6 publications, 7.41%
|
|
The Chemical Society of Japan
1 publication, 1.23%
|
|
Society of Synthetic Organic Chemistry
1 publication, 1.23%
|
|
Taylor & Francis
1 publication, 1.23%
|
|
Springer Nature
1 publication, 1.23%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 1.23%
|
|
5
10
15
20
25
30
35
40
45
|
- 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":[4,5,5,9,8,5,1,5,4,5,6,5,7,8,4],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.94","6.17","6.17","11.11","9.88","6.17","1.23","6.17","4.94","6.17","7.41","6.17","8.64","9.88","4.94"],"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":["Advanced Synthesis and Catalysis","Angewandte Chemie - International Edition","Angewandte Chemie","Organic Letters","Chemical Science","Chemistry - A European Journal","ACS Catalysis","Tetrahedron","Tetrahedron Letters","Journal of the American Chemical Society","Chemical Reviews","Chemical Communications","Organic Chemistry Frontiers","Organic and Biomolecular Chemistry","Chemistry Letters","Yuki Gosei Kagaku Kyokaishi\/Journal of Synthetic Organic Chemistry","Asian Journal of Organic Chemistry","ChemInform","Chemistry - An Asian Journal","Organometallics","Journal of Organic Chemistry","Synthetic Communications","Topics in Current Chemistry","Organic Reaction Mechanisms","Advanced Science","Russian Chemical Reviews"],"ids":[3906,19215,25450,3315,9646,24708,4873,3439,6133,4813,13718,9073,3991,541,6851,3551,9409,25372,10120,1409,8697,1646,23927,42256,4130,23802],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/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\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/ktSZPrGjOMvauY6mn7jk8bqo3Af0S6abv653w90B_medium.webp","\/storage\/images\/resized\/QzzkQMUwda0fYU3txrAv3z24JfXJEjptEQpWMERc_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[10,9,9,8,4,3,3,2,2,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[12.35,11.11,11.11,9.88,4.94,3.7,3.7,2.47,2.47,2.47,2.47,2.47,2.47,2.47,1.23,1.23,1.23,1.23,1.23,1.23,1.23,1.23,1.23,1.23,1.23,1.23],"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","The Chemical Society of Japan","Society of Synthetic Organic Chemistry","Taylor & Francis","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,6950,1303,18,8,9422],"codes":[0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/ktSZPrGjOMvauY6mn7jk8bqo3Af0S6abv653w90B_medium.webp","\/storage\/images\/resized\/QzzkQMUwda0fYU3txrAv3z24JfXJEjptEQpWMERc_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[42,17,10,6,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[51.85,20.99,12.35,7.41,1.23,1.23,1.23,1.23,1.23],"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":[0,0,1,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","1.23","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[1,0,0,1,0,0,0,0,0,1,0,0,0,0,0],"percentage":["1.23","0","0","1.23","0","0","0","0","0","1.23","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,1,0,1,1,0,0,0,0,0,1,0,0,0,0],"percentage":["0","1.23","0","1.23","1.23","0","0","0","0","0","1.23","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[2,4,3,5,4,4,1,5,4,3,5,5,5,8,4],"percentage":["2.47","4.94","3.7","6.17","4.94","4.94","1.23","6.17","4.94","3.7","6.17","6.17","6.17","9.88","4.94"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,1,2,3,1,0,0,0,1,0,0,2,0,0],"percentage":["1.23","0","1.23","2.47","3.7","1.23","0","0","0","1.23","0","0","2.47","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":[0,0,1,1,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","1.23","1.23","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[1,1,0,1,1,0,0,0,0,1,0,0,0,0,0],"percentage":["1.23","1.23","0","1.23","1.23","0","0","0","0","1.23","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[1,0,3,2,0,1,0,0,0,0,1,1,0,0,1],"percentage":["1.23","0","3.7","2.47","0","1.23","0","0","0","0","1.23","1.23","0","0","1.23"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,3,0,3,4,2,1,4,4,2,4,3,4,6,3],"percentage":["1.23","3.7","0","3.7","4.94","2.47","1.23","4.94","4.94","2.47","4.94","3.7","4.94","7.41","3.7"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,1,1,2,3,2,0,1,0,2,1,1,3,2,0],"percentage":["1.23","1.23","1.23","2.47","3.7","2.47","0","1.23","0","2.47","1.23","1.23","3.7","2.47","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
SAITO S. et al. Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes // Angewandte Chemie - International Edition. 2010. Vol. 49. No. 10. pp. 1830-1833.
GOST all authors (up to 50)
Copy
SAITO S., Maeda K., Yamasaki R., Kitamura T., Nakagawa M., Kato K., Azumaya I., Masu H. Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes // Angewandte Chemie - International Edition. 2010. Vol. 49. No. 10. pp. 1830-1833.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/anie.200907052
UR - https://doi.org/10.1002/anie.200907052
TI - Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes
T2 - Angewandte Chemie - International Edition
AU - SAITO, Shinichi
AU - Maeda, Kyotaro
AU - Yamasaki, Ryu
AU - Kitamura, Takuya
AU - Nakagawa, Minami
AU - Kato, Korehito
AU - Azumaya, Isao
AU - Masu, Hyuma
PY - 2010
DA - 2010/03/01 00:00:00
PB - Wiley
SP - 1830-1833
IS - 10
VL - 49
SN - 1433-7851
SN - 1521-3773
ER -
Cite this
BibTex
Copy
@article{2010_SAITO,
author = {Shinichi SAITO and Kyotaro Maeda and Ryu Yamasaki and Takuya Kitamura and Minami Nakagawa and Korehito Kato and Isao Azumaya and Hyuma Masu},
title = {Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes},
journal = {Angewandte Chemie - International Edition},
year = {2010},
volume = {49},
publisher = {Wiley},
month = {mar},
url = {https://doi.org/10.1002/anie.200907052},
number = {10},
pages = {1830--1833},
doi = {10.1002/anie.200907052}
}
Cite this
MLA
Copy
SAITO, Shinichi, et al. “Synthesis of Nine-Membered Carbocycles by the [4+3+2] Cycloaddition Reaction of Ethyl Cyclopropylideneacetate and Dienynes.” Angewandte Chemie - International Edition, vol. 49, no. 10, Mar. 2010, pp. 1830-1833. https://doi.org/10.1002/anie.200907052.