Angewandte Chemie - International Edition, volume 51, issue 1, pages 227-231
Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
Publication type: Journal Article
Publication date: 2011-11-15
Quartile SCImago
Q1
Quartile WOS
Q1
SJR: 5.300
CiteScore: 26.6
Impact factor: 16.1
ISSN: 14337851, 15213773
General Chemistry
Catalysis
Abstract
An efficient method involving a Pd/PCy3 catalyst in combination with a stoichiometric amount of Ag2CO3 has been established for the decarboxylative CH bond arylation of thiophenes to give 2-arylthiophenes (see scheme; Cy=cyclohexyl). Electron-rich, electron-deficient, and heterocyclic benzoic acids can be used as the arylating reagent and a broad range of substituents on the thiophene are tolerated.
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GOST
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Hu P. et al. Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes // Angewandte Chemie - International Edition. 2011. Vol. 51. No. 1. pp. 227-231.
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Hu P., Zhang M., Jie X., Su W. Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes // Angewandte Chemie - International Edition. 2011. Vol. 51. No. 1. pp. 227-231.
Cite this
RIS
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TY - JOUR
DO - 10.1002/anie.201106451
UR - https://doi.org/10.1002/anie.201106451
TI - Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes
T2 - Angewandte Chemie - International Edition
AU - Hu, Peng
AU - Zhang, Min
AU - Jie, Xiaoming
AU - Su, Weiping
PY - 2011
DA - 2011/11/15
PB - Wiley
SP - 227-231
IS - 1
VL - 51
SN - 1433-7851
SN - 1521-3773
ER -
Cite this
BibTex
Copy
@article{2011_Hu,
author = {Peng Hu and Min Zhang and Xiaoming Jie and Weiping Su},
title = {Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes},
journal = {Angewandte Chemie - International Edition},
year = {2011},
volume = {51},
publisher = {Wiley},
month = {nov},
url = {https://doi.org/10.1002/anie.201106451},
number = {1},
pages = {227--231},
doi = {10.1002/anie.201106451}
}
Cite this
MLA
Copy
Hu, Peng, et al. “Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes.” Angewandte Chemie - International Edition, vol. 51, no. 1, Nov. 2011, pp. 227-231. https://doi.org/10.1002/anie.201106451.