Organic Letters, volume 12, issue 5, pages 992-995
Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products
Publication type: Journal Article
Publication date: 2010-02-02
Journal:
Organic Letters
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.2
ISSN: 15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
A Rh(I)-based catalyst system has been developed to promote three types of decarboxylative transformations of arenecarboxylic acids: (1) hydrodecarboxylation, (2) Heck-Mizoroki olefination, and (3) conjugate addition. Scopes of reactions (1) and (2) were studied, and the ligand and reagent dependence of selectivity was explored.
Top-30
Citations by journals
2
4
6
8
10
12
|
|
Organic Letters
12 publications, 10%
|
|
Chemistry - A European Journal
7 publications, 5.83%
|
|
European Journal of Organic Chemistry
7 publications, 5.83%
|
|
Advanced Synthesis and Catalysis
7 publications, 5.83%
|
|
Journal of the American Chemical Society
6 publications, 5%
|
|
Chemical Communications
6 publications, 5%
|
|
Angewandte Chemie - International Edition
5 publications, 4.17%
|
|
Angewandte Chemie
5 publications, 4.17%
|
|
Organic and Biomolecular Chemistry
5 publications, 4.17%
|
|
Tetrahedron Letters
4 publications, 3.33%
|
|
Asian Journal of Organic Chemistry
4 publications, 3.33%
|
|
ACS Catalysis
4 publications, 3.33%
|
|
RSC Advances
4 publications, 3.33%
|
|
Journal of Organic Chemistry
3 publications, 2.5%
|
|
Synthesis
3 publications, 2.5%
|
|
Synlett
3 publications, 2.5%
|
|
Organometallics
2 publications, 1.67%
|
|
Green Chemistry
2 publications, 1.67%
|
|
Dalton Transactions
2 publications, 1.67%
|
|
Chemical Society Reviews
2 publications, 1.67%
|
|
Organic Chemistry Frontiers
2 publications, 1.67%
|
|
New Journal of Chemistry
2 publications, 1.67%
|
|
Journal of Molecular Modeling
1 publication, 0.83%
|
|
Science China Chemistry
1 publication, 0.83%
|
|
Catalysis Communications
1 publication, 0.83%
|
|
Journal of Molecular Structure
1 publication, 0.83%
|
|
ChemCatChem
1 publication, 0.83%
|
|
Applied Organometallic Chemistry
1 publication, 0.83%
|
|
ChemInform
1 publication, 0.83%
|
|
2
4
6
8
10
12
|
Citations by publishers
5
10
15
20
25
30
35
40
45
50
|
|
Wiley
46 publications, 38.33%
|
|
American Chemical Society (ACS)
30 publications, 25%
|
|
Royal Society of Chemistry (RSC)
26 publications, 21.67%
|
|
Elsevier
7 publications, 5.83%
|
|
Thieme
6 publications, 5%
|
|
Springer Nature
3 publications, 2.5%
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 0.83%
|
|
5
10
15
20
25
30
35
40
45
50
|
- 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":[9,11,8,12,17,17,9,6,8,5,3,4,4,6,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["7.5","9.17","6.67","10","14.17","14.17","7.5","5","6.67","4.17","2.5","3.33","3.33","5","0.83"],"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":["Organic Letters","Chemistry - A European Journal","European Journal of Organic Chemistry","Advanced Synthesis and Catalysis","Journal of the American Chemical Society","Chemical Communications","Angewandte Chemie - International Edition","Angewandte Chemie","Organic and Biomolecular Chemistry","Tetrahedron Letters","Asian Journal of Organic Chemistry","ACS Catalysis","RSC Advances","Journal of Organic Chemistry","Synthesis","Synlett","Organometallics","Green Chemistry","Dalton Transactions","Chemical Society Reviews","Organic Chemistry Frontiers","New Journal of Chemistry","Journal of Molecular Modeling","Science China Chemistry","Catalysis Communications","Journal of Molecular Structure","ChemCatChem","Applied Organometallic Chemistry","ChemInform"],"ids":[3315,24708,19472,3906,4813,9073,19215,25450,541,6133,9409,4873,3100,8697,10934,10217,1409,1017,8473,20586,3991,1404,6610,14409,23806,9347,10149,11683,25372],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_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\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_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"],"datasets":[{"label":"","data":[12,7,7,7,6,6,5,5,5,4,4,4,4,3,3,3,2,2,2,2,2,2,1,1,1,1,1,1,1],"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","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[10,5.83,5.83,5.83,5,5,4.17,4.17,4.17,3.33,3.33,3.33,3.33,2.5,2.5,2.5,1.67,1.67,1.67,1.67,1.67,1.67,0.83,0.83,0.83,0.83,0.83,0.83,0.83],"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","Thieme","Springer Nature","Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii"],"ids":[11,40,123,17,135,8,9422],"codes":[0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/9Mus3KG1Tkd7Bwaurt8H3RwWh0CxRlGoO6ng9UK1_medium.webp"],"datasets":[{"label":"","data":[46,30,26,7,6,3,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[38.33,25,21.67,5.83,5,2.5,0.83],"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":[1,0,1,0,0,0,1,1,0,0,0,0,1,0,0],"percentage":["0.83","0","0.83","0","0","0","0.83","0.83","0","0","0","0","0.83","0","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[0,1,0,2,7,4,3,1,0,2,1,0,1,1,0],"percentage":["0","0.83","0","1.67","5.83","3.33","2.5","0.83","0","1.67","0.83","0","0.83","0.83","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[7,10,6,8,9,11,4,3,7,3,1,4,2,5,1],"percentage":["5.83","8.33","5","6.67","7.5","9.17","3.33","2.5","5.83","2.5","0.83","3.33","1.67","4.17","0.83"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,0,1,2,1,2,1,1,1,0,1,0,0,0,0],"percentage":["0.83","0","0.83","1.67","0.83","1.67","0.83","0.83","0.83","0","0.83","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":[1,0,1,0,1,0,2,1,0,0,0,0,1,1,0],"percentage":["0.83","0","0.83","0","0.83","0","1.67","0.83","0","0","0","0","0.83","0.83","0"]},{"label":"Q2","backgroundColor":"rgb(232, 213, 89)","data":[3,3,2,4,10,7,5,3,1,4,2,0,0,2,0],"percentage":["2.5","2.5","1.67","3.33","8.33","5.83","4.17","2.5","0.83","3.33","1.67","0","0","1.67","0"]},{"label":"Q1","backgroundColor":"rgb(164, 207, 99)","data":[4,7,3,5,5,7,1,1,6,1,0,3,3,3,1],"percentage":["3.33","5.83","2.5","4.17","4.17","5.83","0.83","0.83","5","0.83","0","2.5","2.5","2.5","0.83"]},{"label":"Quartile not defined","backgroundColor":"#E5E7EB","data":[1,1,2,3,1,3,1,1,1,0,1,1,0,0,0],"percentage":["0.83","0.83","1.67","2.5","0.83","2.5","0.83","0.83","0.83","0","0.83","0.83","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
SUN Z., Zhang J., Zhao P. Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products // Organic Letters. 2010. Vol. 12. No. 5. pp. 992-995.
GOST all authors (up to 50)
Copy
SUN Z., Zhang J., Zhao P. Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products // Organic Letters. 2010. Vol. 12. No. 5. pp. 992-995.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol100001b
UR - https://doi.org/10.1021/ol100001b
TI - Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products
T2 - Organic Letters
AU - SUN, ZHONGMING
AU - Zhang, Jing
AU - Zhao, Pinjing
PY - 2010
DA - 2010/02/02 00:00:00
PB - American Chemical Society (ACS)
SP - 992-995
IS - 5
VL - 12
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex
Copy
@article{2010_SUN,
author = {ZHONGMING SUN and Jing Zhang and Pinjing Zhao},
title = {Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products},
journal = {Organic Letters},
year = {2010},
volume = {12},
publisher = {American Chemical Society (ACS)},
month = {feb},
url = {https://doi.org/10.1021/ol100001b},
number = {5},
pages = {992--995},
doi = {10.1021/ol100001b}
}
Cite this
MLA
Copy
SUN, ZHONGMING, et al. “Rh(I)-Catalyzed Decarboxylative Transformations of Arenecarboxylic Acids: Ligand- and Reagent-Controlled Selectivity toward Hydrodecarboxylation or Heck−Mizoroki Products.” Organic Letters, vol. 12, no. 5, Feb. 2010, pp. 992-995. https://doi.org/10.1021/ol100001b.