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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4866
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dc.contributor.authorCooper, M.-
dc.contributor.authorLucas, M.-
dc.contributor.authorSeater, J.-
dc.contributor.authorWard, A.-
dc.contributor.authorWilliamson, N.-
dc.date.issued2001-
dc.identifier.citationSynthesis: journal of synthetic organic chemistry, 2001; 2001(4):621-625-
dc.identifier.issn0039-7881-
dc.identifier.issn1437-210X-
dc.identifier.urihttp://hdl.handle.net/2440/4866-
dc.description.abstractN-(1,1-Disubstituted-allyl)anilines are rearranged cleanly and in high yield to 2-(3,3-disubstituted-allyl)anilines using a catalytic amount of p-toluenesulfonic acid in acetonitrile/water (10:1).-
dc.language.isoen-
dc.publisherGeorg Thieme Verlag-
dc.source.urihttp://dx.doi.org/10.1055/s-2001-12349-
dc.titleA convenient method for the aromatic amino-Claisen rearrangement of N(1,1-disubstituted-allyl)anilines-
dc.typeJournal article-
dc.identifier.doi10.1055/s-2001-12349-
pubs.publication-statusPublished-
dc.identifier.orcidWilliamson, N. [0000-0002-0779-7839]-
Appears in Collections:Aurora harvest 2
Chemistry publications

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