Radical mediated-direct conversion of aldehydes into acid bromides

Dong Ho Kang; Tae Young Joo; Warinthorn Chavasiri; Doo Ok Jang

doi:10.1016/j.tetlet.2006.11.013

Radical mediated-direct conversion of aldehydes into acid bromides

Dong Ho Kang, Tae Young Joo, Warinthorn Chavasiri, Doo Ok Jang

Chemistry and Medical Chemistry

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

6 Citations (Scopus)

Abstract

A method of preparing acid bromides directly from aldehydes with Br₃CCO₂Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-withdrawing group and aliphatic aldehydes under reaction conditions.

Original language	English
Pages (from-to)	285-287
Number of pages	3
Journal	Tetrahedron Letters
Volume	48
Issue number	2
DOIs	https://doi.org/10.1016/j.tetlet.2006.11.013
Publication status	Published - 2007 Jan 8

Bibliographical note

Funding Information:
This work was supported by joint research project under the KOSEF-NRCT cooperative program (F01-2004-000-10252-0) and CBMH.

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2006.11.013

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title = "Radical mediated-direct conversion of aldehydes into acid bromides",

abstract = "A method of preparing acid bromides directly from aldehydes with Br3CCO2Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-withdrawing group and aliphatic aldehydes under reaction conditions.",

author = "Kang, {Dong Ho} and Joo, {Tae Young} and Warinthorn Chavasiri and Jang, {Doo Ok}",

note = "Funding Information: This work was supported by joint research project under the KOSEF-NRCT cooperative program (F01-2004-000-10252-0) and CBMH.",

year = "2007",

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doi = "10.1016/j.tetlet.2006.11.013",

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T1 - Radical mediated-direct conversion of aldehydes into acid bromides

AU - Kang, Dong Ho

AU - Joo, Tae Young

AU - Chavasiri, Warinthorn

AU - Jang, Doo Ok

N1 - Funding Information: This work was supported by joint research project under the KOSEF-NRCT cooperative program (F01-2004-000-10252-0) and CBMH.

PY - 2007/1/8

Y1 - 2007/1/8

N2 - A method of preparing acid bromides directly from aldehydes with Br3CCO2Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-withdrawing group and aliphatic aldehydes under reaction conditions.

AB - A method of preparing acid bromides directly from aldehydes with Br3CCO2Et under radical conditions was developed. Aromatic aldehydes with electron-donating group were found to be more reactive than aromatic aldehydes with electron-withdrawing group and aliphatic aldehydes under reaction conditions.

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DO - 10.1016/j.tetlet.2006.11.013

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 2

ER -

Radical mediated-direct conversion of aldehydes into acid bromides

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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