The hydrogenolysis of 1,8-cineole

Helmut M. Hügel, W. R. Roy Jackson, Christine D. Kachel, Ian D. Rae

Research output: Contribution to journalArticleResearchpeer-review

5 Citations (Scopus)

Abstract

Reaction of 1,8-cineole with hydrogen over supported platinum and palladium catalysts gives mixtures of cis- and trans-p-menthanes. p-Cymene is also produced from reactions at higher temperatures over palladium on pumice. Studies of reactions of potential intermediates and of the reaction of 1,8-cineole with deuterium have led to a proposed mechanism for the reaction.

Original languageEnglish
Pages (from-to)1287-1292
Number of pages6
JournalAustralian Journal of Chemistry
Volume30
Issue number6
DOIs
Publication statusPublished - 1 Jan 1977

Cite this

Hügel, H. M., Roy Jackson, W. R., Kachel, C. D., & Rae, I. D. (1977). The hydrogenolysis of 1,8-cineole. Australian Journal of Chemistry, 30(6), 1287-1292. https://doi.org/10.1071/CH9771287
Hügel, Helmut M. ; Roy Jackson, W. R. ; Kachel, Christine D. ; Rae, Ian D. / The hydrogenolysis of 1,8-cineole. In: Australian Journal of Chemistry. 1977 ; Vol. 30, No. 6. pp. 1287-1292.
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Hügel, HM, Roy Jackson, WR, Kachel, CD & Rae, ID 1977, 'The hydrogenolysis of 1,8-cineole', Australian Journal of Chemistry, vol. 30, no. 6, pp. 1287-1292. https://doi.org/10.1071/CH9771287

The hydrogenolysis of 1,8-cineole. / Hügel, Helmut M.; Roy Jackson, W. R.; Kachel, Christine D.; Rae, Ian D.

In: Australian Journal of Chemistry, Vol. 30, No. 6, 01.01.1977, p. 1287-1292.

Research output: Contribution to journalArticleResearchpeer-review

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Hügel HM, Roy Jackson WR, Kachel CD, Rae ID. The hydrogenolysis of 1,8-cineole. Australian Journal of Chemistry. 1977 Jan 1;30(6):1287-1292. https://doi.org/10.1071/CH9771287