Substituent effects in the hydrogenation of Δ1,9-octalins
The presence of the 4α-methyl group in olefin 4 or in conjugated ketone 10 prevents catalytic hydrogenation from the α side, leading exclusively to cis-fused decalins.
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Published in | Canadian journal of chemistry Vol. 62; no. 2; pp. 273 - 276 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Ottawa, Canada
NRC Research Press
01.02.1984
|
Online Access | Get full text |
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Abstract | The presence of the 4α-methyl group in olefin
4
or in conjugated ketone
10
prevents catalytic hydrogenation from the α side, leading exclusively to cis-fused decalins. |
---|---|
AbstractList | The presence of the 4α-methyl group in olefin
4
or in conjugated ketone
10
prevents catalytic hydrogenation from the α side, leading exclusively to cis-fused decalins. |
Abstract_FL | On rapporte que l'hydrogénation catalytique de l'oléfine
4
ou de la cétone conjuguée
10
conduit exclusivement a la cis-décaline correspondante étant donné la présence du groupement méthyle-4α qui empêche la réaction de s'effectuer du côté α de la molécule. [Traduit par le journal] |
Author | Breining, Tibor Schmidt, Cirill |
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ContentType | Journal Article |
DOI | 10.1139/v84-045 |
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EndPage | 276 |
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Snippet | The presence of the 4α-methyl group in olefin
4
or in conjugated ketone
10
prevents catalytic hydrogenation from the α side, leading exclusively to cis-fused... |
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StartPage | 273 |
Title | Substituent effects in the hydrogenation of Δ1,9-octalins |
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