Chirality of products in acid-catalyzed rearrangement of a-pinene
| Autor: | De Stefanis A., Perez G., Tomlinson A.A.G., Ursini O., Lilla E. |
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| Rok vydání: | 2003 |
| Zdroj: | Reaction kinetics and catalysis letters 78 (2003): 267–273. info:cnr-pdr/source/autori:De Stefanis A., Perez G., Tomlinson A.A.G., Ursini O., Lilla E./titolo:Chirality of products in acid-catalyzed rearrangement of a-pinene/doi:/rivista:Reaction kinetics and catalysis letters (Print)/anno:2003/pagina_da:267/pagina_a:273/intervallo_pagine:267–273/volume:78 |
| Popis: | Protonation of (1R)-(+)-a-pinene using gaseous H3+ ions led to a racemic mixture of camphene and limonene, to partial and no racemization, in acidic solution and in solid acids, respectively. |
| Databáze: | OpenAIRE |
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