Autor: |
François Garin, Arlette Solladié-Cavallo, Baram Ahmed, Michel Schmitt |
Rok vydání: |
2005 |
Předmět: |
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Zdroj: |
Comptes Rendus Chimie. 8:1975-1980 |
ISSN: |
1631-0748 |
Popis: |
Heterogeneous hydrogenations of 1-naphthol and 2-naphthol over Ru/Al 2 O 3 -9001 (from Engelhard) are presented. It was found that 1-naphthol provides almost exclusively (98–100%) the cis -decalols (OH equatorial and axial) while the 2-naphthol lead to mixtures of a cis -decalol (OH equatorial) and a trans -decalol (OH equatorial) in 1/1–1/2 ratio where the trans -decalol is major. A rapid and simple 1 H NMR method (based on analysis of the patterns and of the 3 J values obtained from the C H (OH) proton) is described, which allows unambiguous assignment of the diastereomers of 1-decalols and 2-decalols. To cite this article: A. Solladie-Cavallo et al., C. R. Chimie (2005) . |
Databáze: |
OpenAIRE |
Externí odkaz: |
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