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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 19, 1989 - Issue 3-4
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Original Articles

Selective Reduction of Dienones Synthesis of Intermediates for Sesqui-and Diterpenes

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Pages 673-678 | Received 18 Jul 1988, Published online: 23 Oct 2006
 

Abstract

The tricyclic enones 1520, intermediates to several sesqui-and diterpenes, have been synthesised in high yields involving selective hydrogenation of the disubstituted double bonds of the dienones 9-14 respectively in the presence of tris (triphenylphosphine)rhodium(I) chloride catalyst.

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