Dual oxidation/bromination of alkylbenzenes

Marwa M. Aborways; Wesley J. Moran

doi:10.1016/j.tetlet.2016.01.062

Dual oxidation/bromination of alkylbenzenes

Marwa M. Aborways, Wesley J. Moran

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

3 Citations (Scopus)

Abstract

In the presence of sodium bromide and Oxone, a range of alkylbenzene derivatives are brominated and/or oxidized with up to four C-H bonds being functionalized.

Original language	English
Pages (from-to)	983-985
Number of pages	3
Journal	Tetrahedron Letters
Volume	57
Issue number	9
Early online date	22 Jan 2016
DOIs	https://doi.org/10.1016/j.tetlet.2016.01.062
Publication status	Published - 2 Mar 2016

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http://eprints.hud.ac.uk/id/eprint/27194/Licence: CC BY-NC-ND

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title = "Dual oxidation/bromination of alkylbenzenes",

abstract = "In the presence of sodium bromide and Oxone, a range of alkylbenzene derivatives are brominated and/or oxidized with up to four C-H bonds being functionalized.",

keywords = "Aromatic, Bromination, Oxidation",

author = "Aborways, {Marwa M.} and Moran, {Wesley J.}",

year = "2016",

month = mar,

day = "2",

doi = "10.1016/j.tetlet.2016.01.062",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - Dual oxidation/bromination of alkylbenzenes

AU - Aborways, Marwa M.

AU - Moran, Wesley J.

PY - 2016/3/2

Y1 - 2016/3/2

N2 - In the presence of sodium bromide and Oxone, a range of alkylbenzene derivatives are brominated and/or oxidized with up to four C-H bonds being functionalized.

AB - In the presence of sodium bromide and Oxone, a range of alkylbenzene derivatives are brominated and/or oxidized with up to four C-H bonds being functionalized.

KW - Aromatic

KW - Bromination

KW - Oxidation

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U2 - 10.1016/j.tetlet.2016.01.062

DO - 10.1016/j.tetlet.2016.01.062

M3 - Article

AN - SCOPUS:84957430954

VL - 57

SP - 983

EP - 985

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 9

ER -

Dual oxidation/bromination of alkylbenzenes

Abstract

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