Unexpected rearrangement during the gas-phase dehalogenation approach to benzodithiophenes

R Alan Aitken; Adebayo O Oyewale

doi:10.1039/C4RA15004J

Unexpected rearrangement during the gas-phase dehalogenation approach to benzodithiophenes

R Alan Aitken
, Adebayo O Oyewale

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

Abstract

A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates.

Original language	English
Pages (from-to)	19379-19381
Number of pages	3
Journal	RSC Advances
Volume	5
Issue number	25
Early online date	9 Feb 2015
DOIs	https://doi.org/10.1039/C4RA15004J
Publication status	Published - 17 Feb 2015

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aitken2014rscadvances19379
© 2015. The Royal Society of Chemistry. Open Access article. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
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title = "Unexpected rearrangement during the gas-phase dehalogenation approach to benzodithiophenes",

abstract = "A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates.",

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N2 - A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates.

AB - A range of halogenated methylthiophenes undergo dehalogenative condensation upon FVP over magnesium or calcium to give products including benzodithiophenes; in some cases this involves a novel rearrangement by equilibration of alkenylthienyl radicals via thiophene-fused cyclopropylmethyl intermediates.

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DO - 10.1039/C4RA15004J

M3 - Article

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JO - RSC Advances

JF - RSC Advances

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Unexpected rearrangement during the gas-phase dehalogenation approach to benzodithiophenes

Abstract

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