Facile preparation of 2-arylbenzoselenazoles from three components reactions: 2-Chloronitrobenzene, Se, and arylacetic acids

Haifeng Gan; Douglas R. Macfarlane

doi:10.1016/j.tetlet.2019.151393

Facile preparation of 2-arylbenzoselenazoles from three components reactions: 2-Chloronitrobenzene, Se, and arylacetic acids

Haifeng Gan, Douglas R. Macfarlane

School of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

8 Citations (Scopus)

Abstract

A selenium-mediated decarboxylative cyclization of 2-chloronitrobenzene and arylacetic acids to prepare 2-arylbenzoselenazoles has been established under metal-free condition. The reactions proceeded in moderate to good yields with good functional tolerance and gram-scale application.

Original language	English
Article number	151393
Number of pages	4
Journal	Tetrahedron Letters
Volume	61
Issue number	3
DOIs	https://doi.org/10.1016/j.tetlet.2019.151393
Publication status	Published - 16 Jan 2020

Keywords

Arylacetic acid
Benzoselenazoles
Cyclization
Selenium powder

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title = "Facile preparation of 2-arylbenzoselenazoles from three components reactions: 2-Chloronitrobenzene, Se, and arylacetic acids",

abstract = "A selenium-mediated decarboxylative cyclization of 2-chloronitrobenzene and arylacetic acids to prepare 2-arylbenzoselenazoles has been established under metal-free condition. The reactions proceeded in moderate to good yields with good functional tolerance and gram-scale application.",

keywords = "Arylacetic acid, Benzoselenazoles, Cyclization, Selenium powder",

author = "Haifeng Gan and Macfarlane, {Douglas R.}",

note = "Funding Information: We are grateful to the National High Technology Research and Development Program of China (No. 2013AA031901 ) for the financial support. Appendix A Publisher Copyright: {\textcopyright} 2019 Elsevier Ltd",

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T2 - 2-Chloronitrobenzene, Se, and arylacetic acids

AU - Gan, Haifeng

AU - Macfarlane, Douglas R.

N1 - Funding Information: We are grateful to the National High Technology Research and Development Program of China (No. 2013AA031901 ) for the financial support. Appendix A Publisher Copyright: © 2019 Elsevier Ltd

PY - 2020/1/16

Y1 - 2020/1/16

N2 - A selenium-mediated decarboxylative cyclization of 2-chloronitrobenzene and arylacetic acids to prepare 2-arylbenzoselenazoles has been established under metal-free condition. The reactions proceeded in moderate to good yields with good functional tolerance and gram-scale application.

AB - A selenium-mediated decarboxylative cyclization of 2-chloronitrobenzene and arylacetic acids to prepare 2-arylbenzoselenazoles has been established under metal-free condition. The reactions proceeded in moderate to good yields with good functional tolerance and gram-scale application.

KW - Arylacetic acid

KW - Benzoselenazoles

KW - Cyclization

KW - Selenium powder

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DO - 10.1016/j.tetlet.2019.151393

M3 - Article

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SN - 0040-4039

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

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ER -

Facile preparation of 2-arylbenzoselenazoles from three components reactions: 2-Chloronitrobenzene, Se, and arylacetic acids

Abstract

Keywords

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