Cammidge, Andrew N. ORCID: https://orcid.org/0000-0001-7912-4310, Crepy, Karen V. and Fugier, Matthieu
(1997)
Convenient ring-bromination of alkylnaphthalenes using N-bromosuccinimide in acetonitrile.
Synthetic Communications, 27 (23).
pp. 4159-4162.
ISSN 0039-7911
Abstract
1-Alkyl- and 2-alkylnaphthalenes are conveniently brominated in the 4-and 1-positions respectively using N-bromosuccinimide (NBS) in acetonitrile. The reactions are easy to perform and give higher chemical yields and better regioselectivity compared to brominations employing bromine/dichloromethane.
Item Type: | Article |
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Faculty \ School: | Faculty of Science > School of Chemistry |
Depositing User: | Rachel Smith |
Date Deposited: | 24 Nov 2010 14:50 |
Last Modified: | 15 Dec 2022 02:01 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/11005 |
DOI: | 10.1080/00397919708005463 |
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