Advanced Synthesis and Catalysis, volume 364, issue 13, pages 2248-2253
Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines
Publication type: Journal Article
Publication date: 2022-05-24
Journal:
Advanced Synthesis and Catalysis
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.4
ISSN: 16154150, 16154169
General Chemistry
Abstract
Arylation of tertiary aryl and alkyl phosphines bearing 2-cyanoethyl group with aryl(mesityl)iodonium triflates under blue light irradiation followed by retro-Michael reaction of the in situ generated quaternary phosphonium salts initiated by DBU represent a novel efficient and general method for the preparation of distinctly substituted tertiary arylphosphines. An operationally simple, one-pot protocol features mild, transition-metal-free conditions, high selectivity, broad functional group compatibility, as well as scalability and would be applied to substrates with different electronic and steric nature.
Citations by journals
|
1
2
|
|
|
Organic Letters
|
Organic Letters
2 publications, 25%
|
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
1 publication, 12.5%
|
|
Organic Chemistry Frontiers
|
Organic Chemistry Frontiers
1 publication, 12.5%
|
|
Angewandte Chemie
|
Angewandte Chemie
1 publication, 12.5%
|
|
Angewandte Chemie - International Edition
|
Angewandte Chemie - International Edition
1 publication, 12.5%
|
|
Chemistry - A European Journal
|
Chemistry - A European Journal
1 publication, 12.5%
|
|
ChemCatChem
|
ChemCatChem
1 publication, 12.5%
|
|
1
2
|
Citations by publishers
|
1
2
3
4
5
|
|
|
Wiley
|
Wiley
5 publications, 62.5%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
2 publications, 25%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
1 publication, 12.5%
|
|
1
2
3
4
5
|
- 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":[2023,2024],"ids":[0,0],"codes":[0,0],"imageUrls":["",""],"datasets":[{"label":"Citations number","data":[6,2],"backgroundColor":["#3B82F6","#3B82F6"],"percentage":["75","25"],"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":["Organic Letters","Advanced Synthesis and Catalysis","Organic Chemistry Frontiers","Angewandte Chemie","Angewandte Chemie - International Edition","Chemistry - A European Journal","ChemCatChem"],"ids":[3315,3906,3991,25450,19215,24708,10149],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_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"],"datasets":[{"label":"","data":[2,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[25,12.5,12.5,12.5,12.5,12.5,12.5],"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":["Wiley","American Chemical Society (ACS)","Royal Society of Chemistry (RSC)"],"ids":[11,40,123],"codes":[0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp"],"datasets":[{"label":"","data":[5,2,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6"],"percentage":[62.5,25,12.5],"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
Bugaenko D. I. Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines // Advanced Synthesis and Catalysis. 2022. Vol. 364. No. 13. pp. 2248-2253.
GOST all authors (up to 50)
Copy
Bugaenko D. I. Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines // Advanced Synthesis and Catalysis. 2022. Vol. 364. No. 13. pp. 2248-2253.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/adsc.202200309
UR - https://doi.org/10.1002%2Fadsc.202200309
TI - Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines
T2 - Advanced Synthesis and Catalysis
AU - Bugaenko, Dmitry I
PY - 2022
DA - 2022/05/24 00:00:00
PB - Wiley
SP - 2248-2253
IS - 13
VL - 364
SN - 1615-4150
SN - 1615-4169
ER -
Cite this
BibTex
Copy
@article{2022_Bugaenko,
author = {Dmitry I Bugaenko},
title = {Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines},
journal = {Advanced Synthesis and Catalysis},
year = {2022},
volume = {364},
publisher = {Wiley},
month = {may},
url = {https://doi.org/10.1002%2Fadsc.202200309},
number = {13},
pages = {2248--2253},
doi = {10.1002/adsc.202200309}
}
Cite this
MLA
Copy
Bugaenko, Dmitry I.. “Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines.” Advanced Synthesis and Catalysis, vol. 364, no. 13, May. 2022, pp. 2248-2253. https://doi.org/10.1002%2Fadsc.202200309.
Profiles