β-Hydroxy carbocation intermediates in solvolyses of di- and tetra-hydronaphthalene substrates
Solvolysis of trichloroacetate esters of 2-methoxy-1,2-dihydro-1-naphthols shows a remarkably large difference in rates between the cis and trans isomers, kcis/ktrans = 1800 in aqueous acetonitrile. This mirrors the behaviour of the acid-catalysed dehydration of cis- and trans-naphthalene-1,2-dihydr...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Beilstein-Institut
2010-11-01
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| Series: | Beilstein Journal of Organic Chemistry |
| Assuntos: | |
| Acceso en liña: | https://doi.org/10.3762/bjoc.6.118 |
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