Regioselective bromination of 1,4-dimethoxy-2,3-dimethylbenzene and conversion into sulfur-functionalised benzoquinones

Aitken, Robert Alan; Jethwa, Siddharth Janak; Richardson, Neville Vincent; Slawin, Alexandra Martha Zoya

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dc.contributor.author	Aitken, Robert Alan
dc.contributor.author	Jethwa, Siddharth Janak
dc.contributor.author	Richardson, Neville Vincent
dc.contributor.author	Slawin, Alexandra Martha Zoya
dc.date.accessioned	2017-02-28T00:32:44Z
dc.date.available	2017-02-28T00:32:44Z
dc.date.issued	2016-03-11
dc.identifier.citation	Aitken , R A , Jethwa , S J , Richardson , N V & Slawin , A M Z 2016 , ' Regioselective bromination of 1,4-dimethoxy-2,3-dimethylbenzene and conversion into sulfur-functionalised benzoquinones ' , Tetrahedron Letters , vol. 57 , no. 14 , pp. 1563-1566 . https://doi.org/10.1016/j.tetlet.2016.02.091	en
dc.identifier.issn	0040-4039
dc.identifier.other	PURE: 241226968
dc.identifier.other	PURE UUID: 2f962e80-9d5f-40ea-8655-2be217adc2b2
dc.identifier.other	Scopus: 85030259503
dc.identifier.other	ORCID: /0000-0001-6959-5311/work/34857571
dc.identifier.other	ORCID: /0000-0002-9527-6418/work/56861785
dc.identifier.other	WOS: 000372945300011
dc.identifier.uri	http://hdl.handle.net/10023/10376
dc.description.abstract	The NBS bromination of 1,4-dimethoxy-2,3-dimethylbenzene has been examined under a variety of conditions in both 1,1,1-trichloroethane and benzotrifluoride. Four different bromination products have been isolated including the previously unknown 1-bromo-4-bromomethyl-2,5-dimethoxy-3-methylbenzene whose single crystal X-ray structure is presented. The synthetically useful 2,3-bis(bromomethyl)-1,4-dimethoxybenzene is readily prepared using either solvent and it has been converted into new sulfur-containing quinone derivatives
dc.format.extent	4
dc.language.iso	eng
dc.relation.ispartof	Tetrahedron Letters	en
dc.rights	Copyright © 2016 Elsevier Ltd. All rights reserved. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at https://dx.doi.org/10.1016/j.tetlet.2016.02.091	en
dc.subject	Bromination	en
dc.subject	Benzotrifluoride	en
dc.subject	Solvent effects	en
dc.subject	X-ray structures	en
dc.subject	QD Chemistry	en
dc.subject	DAS	en
dc.subject.lcc	QD	en
dc.title	Regioselective bromination of 1,4-dimethoxy-2,3-dimethylbenzene and conversion into sulfur-functionalised benzoquinones	en
dc.type	Journal article	en
dc.description.version	Postprint	en
dc.contributor.institution	University of St Andrews. School of Chemistry	en
dc.contributor.institution	University of St Andrews. EaSTCHEM	en
dc.identifier.doi	https://doi.org/10.1016/j.tetlet.2016.02.091
dc.description.status	Peer reviewed	en
dc.date.embargoedUntil	2017-02-27
dc.identifier.url	http://www.sciencedirect.com/science/article/pii/S0040403916302003#appd002	en

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