Synthetic Communications, volume 39, issue 21, pages 3856-3866
Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition
Vipraja V Vaidya
1
,
Karuna S Wankhede
1
,
Susheel J Nara
1
,
Manikrao M Salunkhe
2
,
Girish K. Trivedi
1
1
a Department of Chemistry , Institute of Science , Mumbai, India
|
Publication type: Journal Article
Publication date: 2009-10-07
Journal:
Synthetic Communications
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 2.1
ISSN: 00397911, 15322432
Organic Chemistry
Abstract
Abstract 1,3-Dipolar cycloaddition was utilized as a tool to conjugate the 1,4-benzodioxane moiety with several biologically active compounds such as steroid, sugar, and other aromatic scaffolds via isoxazole or triazole bridge. The propynyl ether of 2-hydroxymethyl-1,4-benzodioxane underwent 1,3-dipolar cycloadditions smoothly with different in situ generated nitrile oxides in good yields. The triazole conjugate of 1,4-benzodioxane was synthesized via click chemistry.
Top-30
Citations by journals
1
2
|
|
Russian Chemical Reviews
2 publications, 22.22%
|
|
Tetrahedron
2 publications, 22.22%
|
|
European Journal of Organic Chemistry
2 publications, 22.22%
|
|
ChemInform
1 publication, 11.11%
|
|
1
2
|
Citations by publishers
1
2
3
|
|
Wiley
3 publications, 33.33%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 publications, 22.22%
|
|
Elsevier
2 publications, 22.22%
|
|
1
2
3
|
- 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":[1,0,1,0,1,1,2,0,0,0,0,0,2,0,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["11.11",0,"11.11",0,"11.11","11.11","22.22",0,0,0,0,0,"22.22",0,"11.11"],"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":["Russian Chemical Reviews","Tetrahedron","European Journal of Organic Chemistry","ChemInform"],"ids":[23802,3439,19472,25372],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp"],"datasets":[{"label":"","data":[2,2,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[22.22,22.22,22.22,11.11],"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","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii","Elsevier"],"ids":[11,9422,17],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp"],"datasets":[{"label":"","data":[3,2,2],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":[33.33,22.22,22.22],"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":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,0,1,0,2,0,0,0,0,0,0,0,0],"percentage":["0","0","11.11","0","11.11","0","22.22","0","0","0","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,0,0,0,0,1,0,0,0,0,0,0,0,0,1],"percentage":["0","0","0","0","0","11.11","0","0","0","0","0","0","0","0","11.11"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,0,0,0,0,0,0,2,0,0],"percentage":["11.11","0","0","0","0","0","0","0","0","0","0","0","22.22","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":[0,0,0,0,0,0,2,0,0,0,0,0,0,0,0],"percentage":["0","0","0","0","0","0","22.22","0","0","0","0","0","0","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,0,1,0,1,0,0,0,0,0,0,0,0,0,0],"percentage":["0","0","11.11","0","11.11","0","0","0","0","0","0","0","0","0","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[0,0,0,0,0,1,0,0,0,0,0,0,0,0,1],"percentage":["0","0","0","0","0","11.11","0","0","0","0","0","0","0","0","11.11"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,0,0,0,0,0,0,0,0,2,0,0],"percentage":["11.11","0","0","0","0","0","0","0","0","0","0","0","22.22","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
Vaidya V. V. et al. Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition // Synthetic Communications. 2009. Vol. 39. No. 21. pp. 3856-3866.
GOST all authors (up to 50)
Copy
Vaidya V. V., Wankhede K. S., Nara S. J., Salunkhe M. M., Trivedi G. K. Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition // Synthetic Communications. 2009. Vol. 39. No. 21. pp. 3856-3866.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1080/00397910902838979
UR - https://doi.org/10.1080/00397910902838979
TI - Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition
T2 - Synthetic Communications
AU - Vaidya, Vipraja V
AU - Wankhede, Karuna S
AU - Nara, Susheel J
AU - Salunkhe, Manikrao M
AU - Trivedi, Girish K.
PY - 2009
DA - 2009/10/07 00:00:00
PB - Taylor & Francis
SP - 3856-3866
IS - 21
VL - 39
SN - 0039-7911
SN - 1532-2432
ER -
Cite this
BibTex
Copy
@article{2009_Vaidya,
author = {Vipraja V Vaidya and Karuna S Wankhede and Susheel J Nara and Manikrao M Salunkhe and Girish K. Trivedi},
title = {Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition},
journal = {Synthetic Communications},
year = {2009},
volume = {39},
publisher = {Taylor & Francis},
month = {oct},
url = {https://doi.org/10.1080/00397910902838979},
number = {21},
pages = {3856--3866},
doi = {10.1080/00397910902838979}
}
Cite this
MLA
Copy
Vaidya, Vipraja V., et al. “Synthesis of Isoxazole Conjugates of 1,4-Benzodioxane Moiety via Intermolecular 1,3-Dipolar Cycloaddition.” Synthetic Communications, vol. 39, no. 21, Oct. 2009, pp. 3856-3866. https://doi.org/10.1080/00397910902838979.