Journal of Organic Chemistry, volume 87, issue 9, pages 6459-6470
An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones
Publication type: Journal Article
Publication date: 2022-04-14
Journal:
Journal of Organic Chemistry
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
Abstract
The synthesis of 5-aryl- and 4-aryl/hetaryl/cyclopropyl/alkynyl-5-aryl-1H-pyrrole-2,3-diones by formal isomerization of isoxazole-5-carbaldehydes mediated Mo(CO)6 in wet MeCN has been developed. The resulting 1H-pyrrole-2,3-diones are good precursors for substituted 1H-pyrrolo[2,3-b]quinoxalines.
Citations by journals
1
2
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
2 publications, 28.57%
|
Progress in Heterocyclic Chemistry
|
Progress in Heterocyclic Chemistry
2 publications, 28.57%
|
Tetrahedron Letters
|
Tetrahedron Letters
1 publication, 14.29%
|
Organic and Biomolecular Chemistry
|
Organic and Biomolecular Chemistry
1 publication, 14.29%
|
Russian Journal of General Chemistry
|
Russian Journal of General Chemistry
1 publication, 14.29%
|
1
2
|
Citations by publishers
1
2
3
|
|
Elsevier
|
Elsevier
3 publications, 42.86%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
2 publications, 28.57%
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 14.29%
|
Pleiades Publishing
|
Pleiades Publishing
1 publication, 14.29%
|
1
2
3
|
- We do not take into account publications that 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":[2022,2023],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[1,6],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["14.29","85.71"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"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","Progress in Heterocyclic Chemistry","Tetrahedron Letters","Organic and Biomolecular Chemistry","Russian Journal of General Chemistry"],"ids":[8697,17224,6133,541,13581],"codes":[0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp"],"datasets":[{"label":"","data":[2,2,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[28.57,28.57,14.29,14.29,14.29],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"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":["Elsevier","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)","Pleiades Publishing"],"ids":[17,40,123,101],"codes":[0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/oZgeErrVFhuDksyqFURLvYS1wtVSBWczh001igGo_medium.webp"],"datasets":[{"label":"","data":[3,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[42.86,28.57,14.29,14.29],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Galenko E. E. et al. An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones // Journal of Organic Chemistry. 2022. Vol. 87. No. 9. pp. 6459-6470.
GOST all authors (up to 50)
Copy
Galenko E. E., Puzyk A. M., Novikov M. S., Khlebnikov A. F. An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones // Journal of Organic Chemistry. 2022. Vol. 87. No. 9. pp. 6459-6470.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/acs.joc.2c00386
UR - https://doi.org/10.1021%2Facs.joc.2c00386
TI - An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones
T2 - Journal of Organic Chemistry
AU - Novikov, Mikhail S.
AU - Puzyk, Aleksandra M
AU - Galenko, Ekaterina E
AU - Khlebnikov, Alexander F
PY - 2022
DA - 2022/04/14 00:00:00
PB - American Chemical Society (ACS)
SP - 6459-6470
IS - 9
VL - 87
SN - 0022-3263
SN - 1520-6904
ER -
Cite this
BibTex
Copy
@article{2022_Galenko,
author = {Mikhail S. Novikov and Aleksandra M Puzyk and Ekaterina E Galenko and Alexander F Khlebnikov},
title = {An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones},
journal = {Journal of Organic Chemistry},
year = {2022},
volume = {87},
publisher = {American Chemical Society (ACS)},
month = {apr},
url = {https://doi.org/10.1021%2Facs.joc.2c00386},
number = {9},
pages = {6459--6470},
doi = {10.1021/acs.joc.2c00386}
}
Cite this
MLA
Copy
Galenko, Ekaterina E., et al. “An Isoxazole Strategy for Molybdenum-Mediated Synthesis of 5-Mono- and 4,5-Disubstituted 1 H-Pyrrole-2,3-diones.” Journal of Organic Chemistry, vol. 87, no. 9, Apr. 2022, pp. 6459-6470. https://doi.org/10.1021%2Facs.joc.2c00386.