Journal of Organic Chemistry, volume 74, issue 15, pages 5636-5639
Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols
Publication type: Journal Article
Publication date: 2009-06-26
Journal:
Journal of Organic Chemistry
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
Abstract
1-Naphthaldehydes and 3-oxabicyclo[3.1.0]hexan-2-ols can be prepared, respectively, by the intramolecular alkylation and cyclization of (E)-2-(arylmethylene)cyclopropylaldehyde 1 mediated by different organo-selenium reagents. The properties of selenium reagents may play an important role in the reactions. A rationale for these transformations is proposed.
Top-30
Citations by journals
|
1
|
|
|
Beilstein Journal of Organic Chemistry
1 publication, 4.35%
|
|
|
Journal of Organometallic Chemistry
1 publication, 4.35%
|
|
|
Tetrahedron Letters
1 publication, 4.35%
|
|
|
European Journal of Organic Chemistry
1 publication, 4.35%
|
|
|
Advanced Synthesis and Catalysis
1 publication, 4.35%
|
|
|
ChemInform
1 publication, 4.35%
|
|
|
Journal of the American Chemical Society
1 publication, 4.35%
|
|
|
Journal of Organic Chemistry
1 publication, 4.35%
|
|
|
Chemical Reviews
1 publication, 4.35%
|
|
|
ACS Catalysis
1 publication, 4.35%
|
|
|
Organic Letters
1 publication, 4.35%
|
|
|
Organic and Biomolecular Chemistry
1 publication, 4.35%
|
|
|
Chemical Society Reviews
1 publication, 4.35%
|
|
|
Organic Preparations and Procedures International
1 publication, 4.35%
|
|
|
Synthetic Communications
1 publication, 4.35%
|
|
|
Russian Chemical Reviews
1 publication, 4.35%
|
|
|
1
|
Citations by publishers
|
1
2
3
4
5
6
|
|
|
Wiley
6 publications, 26.09%
|
|
|
American Chemical Society (ACS)
5 publications, 21.74%
|
|
|
Elsevier
4 publications, 17.39%
|
|
|
Royal Society of Chemistry (RSC)
2 publications, 8.7%
|
|
|
Taylor & Francis
2 publications, 8.7%
|
|
|
Beilstein-Institut
1 publication, 4.35%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 4.35%
|
|
|
1
2
3
4
5
6
|
- 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":[1,4,2,1,4,3,2,1,0,4,0,0,0,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["4.35","17.39","8.7","4.35","17.39","13.04","8.7","4.35",0,"17.39",0,0,0,0,"4.35"],"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":["Beilstein Journal of Organic Chemistry","Journal of Organometallic Chemistry","Tetrahedron Letters","European Journal of Organic Chemistry","Advanced Synthesis and Catalysis","ChemInform","Journal of the American Chemical Society","Journal of Organic Chemistry","Chemical Reviews","ACS Catalysis","Organic Letters","Organic and Biomolecular Chemistry","Chemical Society Reviews","Organic Preparations and Procedures International","Synthetic Communications","Russian Chemical Reviews"],"ids":[21928,11834,6133,19472,3906,25372,4813,8697,13718,4873,3315,541,20586,5076,1646,23802],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_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\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_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\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35,4.35],"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)","Elsevier","Royal Society of Chemistry (RSC)","Taylor & Francis","Beilstein-Institut","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,17,123,18,6139,9422],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[6,5,4,2,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[26.09,21.74,17.39,8.7,8.7,4.35,4.35],"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":[0,1,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","4.35","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,1,0,0,0,0,1,0,0,1,0,0,0,0,0],"percentage":["0","4.35","0","0","0","0","4.35","0","0","4.35","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,0,0,0,0,1,0,0,1,0,0,0,0,0],"percentage":["0","0","0","0","0","0","4.35","0","0","4.35","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,0,1,0,2,2,0,1,0,2,0,0,0,0,1],"percentage":["0","0","4.35","0","8.7","8.7","0","4.35","0","8.7","0","0","0","0","4.35"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,2,1,1,2,1,0,0,0,0,0,0,0,0,0],"percentage":["4.35","8.7","4.35","4.35","8.7","4.35","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":[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":[0,1,0,0,0,0,1,0,0,1,0,0,0,0,0],"percentage":["0","4.35","0","0","0","0","4.35","0","0","4.35","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,1,0,0,0,0,1,1,0,1,0,0,0,0,0],"percentage":["0","4.35","0","0","0","0","4.35","4.35","0","4.35","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,0,1,0,2,2,0,0,0,2,0,0,0,0,1],"percentage":["0","0","4.35","0","8.7","8.7","0","0","0","8.7","0","0","0","0","4.35"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,2,1,1,2,1,0,0,0,0,0,0,0,0,0],"percentage":["4.35","8.7","4.35","4.35","8.7","4.35","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
Miao M., Huang X. Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols // Journal of Organic Chemistry. 2009. Vol. 74. No. 15. pp. 5636-5639.
GOST all authors (up to 50)
Copy
Miao M., Huang X. Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols // Journal of Organic Chemistry. 2009. Vol. 74. No. 15. pp. 5636-5639.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/jo900805a
UR - https://doi.org/10.1021/jo900805a
TI - Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols
T2 - Journal of Organic Chemistry
AU - Miao, Maozhong
AU - Huang, Xian
PY - 2009
DA - 2009/06/26 00:00:00
PB - American Chemical Society (ACS)
SP - 5636-5639
IS - 15
VL - 74
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex
Copy
@article{2009_Miao,
author = {Maozhong Miao and Xian Huang},
title = {Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols},
journal = {Journal of Organic Chemistry},
year = {2009},
volume = {74},
publisher = {American Chemical Society (ACS)},
month = {jun},
url = {https://doi.org/10.1021/jo900805a},
number = {15},
pages = {5636--5639},
doi = {10.1021/jo900805a}
}
Cite this
MLA
Copy
Miao, Maozhong, et al. “Organo-Selenium Induced Radical Ring-Opening Intramolecular Cyclization or Electrophilic Cyclization of 2- (Arylmethylene)cyclopropylaldehyde: A Tunable Synthesis of 1-Naphthaldehydes or 3-Oxabicyclo[3.1.0]hexan-2-ols.” Journal of Organic Chemistry, vol. 74, no. 15, Jun. 2009, pp. 5636-5639. https://doi.org/10.1021/jo900805a.