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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Bibliographic Details
Published inCanadian journal of chemistry Vol. 62; no. 2; pp. 273 - 276
Main Authors Schmidt, Cirill, Breining, Tibor
Format Journal Article
LanguageEnglish
Published Ottawa, Canada NRC Research Press 01.02.1984
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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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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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Title Substituent effects in the hydrogenation of Δ1,9-octalins
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