Advanced Synthesis and Catalysis, volume 359, issue 10, pages 1678-1683
Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles
Publication type: Journal Article
Publication date: 2017-04-10
Journal:
Advanced Synthesis and Catalysis
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.4
ISSN: 16154150, 16154169
General Chemistry
Abstract
Formylcyclopropanes undergo activation in the presence of an N-heterocyclic carbene catalyst generating a donor-acceptor cyclopropane intermediate with the ability to undergo ring-opening followed by formal [4+2] cycloaddition with alkylideneoxindoles. This enables the direct enantio- and diastereoselective synthesis of tetrahydropyrano[2,3-b]indoles through the use of a chiral NHC catalyst.
Top-30
Citations by journals
|
1
2
3
4
5
6
7
|
|
|
Journal of Organic Chemistry
7 publications, 17.5%
|
|
|
Advanced Synthesis and Catalysis
3 publications, 7.5%
|
|
|
Chemical Record
2 publications, 5%
|
|
|
Catalysts
2 publications, 5%
|
|
|
Chinese Chemical Letters
2 publications, 5%
|
|
|
ChemCatChem
2 publications, 5%
|
|
|
ChemistrySelect
2 publications, 5%
|
|
|
Organic Chemistry Frontiers
2 publications, 5%
|
|
|
Science China Chemistry
1 publication, 2.5%
|
|
|
Molecules
1 publication, 2.5%
|
|
|
Tetrahedron
1 publication, 2.5%
|
|
|
Green Synthesis and Catalysis
1 publication, 2.5%
|
|
|
Angewandte Chemie
1 publication, 2.5%
|
|
|
Angewandte Chemie - International Edition
1 publication, 2.5%
|
|
|
European Journal of Organic Chemistry
1 publication, 2.5%
|
|
|
Chemistry - A European Journal
1 publication, 2.5%
|
|
|
Asian Journal of Organic Chemistry
1 publication, 2.5%
|
|
|
Chemical Reviews
1 publication, 2.5%
|
|
|
Chinese Journal of Organic Chemistry
1 publication, 2.5%
|
|
|
RSC Advances
1 publication, 2.5%
|
|
|
Catalysis Science and Technology
1 publication, 2.5%
|
|
|
Organic and Biomolecular Chemistry
1 publication, 2.5%
|
|
|
New Journal of Chemistry
1 publication, 2.5%
|
|
|
Tetrahedron Chem
1 publication, 2.5%
|
|
|
Russian Chemical Reviews
1 publication, 2.5%
|
|
|
1
2
3
4
5
6
7
|
Citations by publishers
|
2
4
6
8
10
12
14
|
|
|
Wiley
14 publications, 35%
|
|
|
American Chemical Society (ACS)
8 publications, 20%
|
|
|
Royal Society of Chemistry (RSC)
6 publications, 15%
|
|
|
Elsevier
5 publications, 12.5%
|
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
3 publications, 7.5%
|
|
|
Springer Nature
1 publication, 2.5%
|
|
|
Shanghai Institute of Organic Chemistry
1 publication, 2.5%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 2.5%
|
|
|
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":[2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","",""],"datasets":[{"label":"Citations number","data":[3,7,1,7,5,4,10,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["7.5","17.5","2.5","17.5","12.5","10","25","7.5"],"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":["Journal of Organic Chemistry","Advanced Synthesis and Catalysis","Chemical Record","Catalysts","Chinese Chemical Letters","ChemCatChem","ChemistrySelect","Organic Chemistry Frontiers","Science China Chemistry","Molecules","Tetrahedron","Green Synthesis and Catalysis","Angewandte Chemie","Angewandte Chemie - International Edition","European Journal of Organic Chemistry","Chemistry - A European Journal","Asian Journal of Organic Chemistry","Chemical Reviews","Chinese Journal of Organic Chemistry","RSC Advances","Catalysis Science and Technology","Organic and Biomolecular Chemistry","New Journal of Chemistry","Tetrahedron Chem","Russian Chemical Reviews"],"ids":[8697,3906,22413,3739,20341,10149,8021,3991,14409,1770,3439,26555,25450,19215,19472,24708,9409,13718,11696,3100,2605,541,1404,36165,23802],"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],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_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\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/6EJSsoiR4fNMNMPFBpMh5yKuYKcPXJDQKvKVeEMy_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[7,3,2,2,2,2,2,2,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[17.5,7.5,5,5,5,5,5,5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5,2.5],"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","Multidisciplinary Digital Publishing Institute (MDPI)","Springer Nature","Shanghai Institute of Organic Chemistry","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,202,8,8960,9422],"codes":[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\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/6EJSsoiR4fNMNMPFBpMh5yKuYKcPXJDQKvKVeEMy_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[14,8,6,5,3,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[35,20,15,12.5,7.5,2.5,2.5,2.5],"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":[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],"percentage":["0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,0,0,0,1,0],"percentage":["0","0","0","0","0","0","2.5","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,2,0,3,2,1,1,1],"percentage":["0","5","0","7.5","5","2.5","2.5","2.5"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[3,5,1,4,3,2,7,2],"percentage":["7.5","12.5","2.5","10","7.5","5","17.5","5"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[0,0,0,0,0,1,1,0],"percentage":["0","0","0","0","0","2.5","2.5","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":[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],"percentage":["0","0","0","0","0","0","0","0"]},{"label":"Q3","backgroundColor":"rgb(251, 163,83)","data":[0,0,0,2,1,0,1,0],"percentage":["0","0","0","5","2.5","0","2.5","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[1,3,1,1,2,1,2,1],"percentage":["2.5","7.5","2.5","2.5","5","2.5","5","2.5"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[1,4,0,4,1,2,6,2],"percentage":["2.5","10","0","10","2.5","5","15","5"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,0,0,1,1,1,0],"percentage":["2.5","0","0","0","2.5","2.5","2.5","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
Prieto L. et al. Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles // Advanced Synthesis and Catalysis. 2017. Vol. 359. No. 10. pp. 1678-1683.
GOST all authors (up to 50)
Copy
Prieto L., Sánchez Díez E., Uria U., Reyes E., Carrillo L., Vicario J. L. Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles // Advanced Synthesis and Catalysis. 2017. Vol. 359. No. 10. pp. 1678-1683.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/adsc.201700198
UR - https://doi.org/10.1002/adsc.201700198
TI - Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles
T2 - Advanced Synthesis and Catalysis
AU - Sánchez Díez, Eduardo
AU - Prieto, Liher
AU - Uria, Uxue
AU - Reyes, Efraim
AU - Carrillo, Luisa
AU - Vicario, Jose Luis
PY - 2017
DA - 2017/04/10 00:00:00
PB - Wiley
SP - 1678-1683
IS - 10
VL - 359
SN - 1615-4150
SN - 1615-4169
ER -
Cite this
BibTex
Copy
@article{2017_Prieto,
author = {Eduardo Sánchez Díez and Liher Prieto and Uxue Uria and Efraim Reyes and Luisa Carrillo and Jose Luis Vicario},
title = {Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles},
journal = {Advanced Synthesis and Catalysis},
year = {2017},
volume = {359},
publisher = {Wiley},
month = {apr},
url = {https://doi.org/10.1002/adsc.201700198},
number = {10},
pages = {1678--1683},
doi = {10.1002/adsc.201700198}
}
Cite this
MLA
Copy
Prieto, Liher, et al. “Catalytic Generation of Donor-Acceptor Cyclopropanes under N -Heterocyclic Carbene Activation and their Stereoselective Reaction with Alkylideneoxindoles.” Advanced Synthesis and Catalysis, vol. 359, no. 10, Apr. 2017, pp. 1678-1683. https://doi.org/10.1002/adsc.201700198.