Angewandte Chemie - International Edition

, том 51 , издание 1 , страницы 227-231

Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes

Тип публикации: Journal Article

Дата публикации: 2011-11-15

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Angewandte Chemie - International Edition

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SJR: 5.495

CiteScore: 27.6

Impact factor: 16.9

ISSN: 14337851, 15213773

DOI: 10.1002/anie.201106451

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PubMed ID: 22086842

General Chemistry

Catalysis

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An efficient method involving a Pd/PCy3 catalyst in combination with a stoichiometric amount of Ag2CO3 has been established for the decarboxylative CH 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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Hu P. et al. Palladium-Catalyzed Decarboxylative CH 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 CH Bond Arylation of Thiophenes // Angewandte Chemie - International Edition. 2011. Vol. 51. No. 1. pp. 227-231.

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TY - JOUR

DO - 10.1002/anie.201106451

UR - https://doi.org/10.1002/anie.201106451

TI - Palladium-Catalyzed Decarboxylative CH 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

PMID - 22086842

SN - 1433-7851

SN - 1521-3773

ER -

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@article{2011_Hu,

author = {Peng Hu and Min Zhang and Xiaoming Jie and Weiping Su},

title = {Palladium-Catalyzed Decarboxylative CH 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}

}

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Hu, Peng, et al. “Palladium-Catalyzed Decarboxylative CH Bond Arylation of Thiophenes.” Angewandte Chemie - International Edition, vol. 51, no. 1, Nov. 2011, pp. 227-231. https://doi.org/10.1002/anie.201106451.

Издатель

Wiley

Журнал

Angewandte Chemie - International Edition

SCImago Q1

Tоп 10% SCImago

БС1