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Showing papers on "Terpene published in 1982"


Journal ArticleDOI
TL;DR: Results of toxicity tests with several congeners of R -(+)-pulegone strongly implicated the α-isopropylidene ketone group as the structural unit required for eliciting hepatotoxicity, although the configurational orientation of the methyl group can modulate the hepatotoxic response.

133 citations



Journal ArticleDOI
TL;DR: In this paper, samples were obtained of the volatile essential oils of the two types of curry leaf, Murraya koenigii and Pandanus latifolius, which contained mainly terpenes and sesquiterpene hydrocarbons.

50 citations


Journal ArticleDOI
TL;DR: This article investigated the volatile components in botrytized grape must and transformation of terpenoids in terpene-supplemented grape must by Botrytis cinerea.
Abstract: Experiments were done to investigate the volatile components in botrytized grape must and transformation of terpenoids in terpene-supplemented grape must by Botrytis cinerea Twenty-eight compounds were identified in the volatile concentrate of botrytized must with a combined gas chromatograph-mass spectrometer No terpenoids were detected in the concentrate Linalool or terpinen-4-ol decreased a lot when Botrytis cinerea was cultured in the must with these terpenes for 15 days In linalool-supplemented botrytized must 9 identified and 3 unidentified terpenes were found, while only geranial was detected in terpinen-4-ol-supplemented botrytized must Botrytis cinerea did not produce terpenoid in grape must without terpenes, but transformed linalool added to grape must into some other monoterpenes

23 citations


Patent
14 Oct 1982
TL;DR: In this paper, a process for the conversion of terpenes to limonene which comprises contacting at least one terpene, selected from the group comprised of mono- and bi-cyclic unsaturated hydrocarbons having the formula C10 H16 with an alkali metal sulfide catalyst on a support at a temperature of 300° to 450° C.
Abstract: There is disclosed a process for the conversion of terpenes to limonene which comprises contacting at least one terpene, selected from the group comprised of mono- and bi-cyclic unsaturated hydrocarbons having the formula C10 H16 with an alkali metal sulfide catalyst on a support at a temperature of 300° to 450° C.

21 citations


Journal ArticleDOI
TL;DR: In this article, a stereoselective total synthesis of (±)-cubitene, a diterpene isolated from termite soldiers, and its stereisomer has been achieved utilizing the anion-induced intramolecular cyclization.

19 citations



Journal ArticleDOI
TL;DR: Linalyl pyrophosphate is a sterically plausible precursor of cyclic hydrocarbons, but the present data support only its role as an alternative substrate and not as an obligatory free intermediate in terpene biosynthesis.

16 citations


Book ChapterDOI
01 Jan 1982

13 citations


Journal ArticleDOI
TL;DR: In this article, a new terpene glucoside, Loliolide-β-d-glucopyranoside from Flue-cured Tobacco, was isolated.
Abstract: (1982). Isolation of a New Terpene Glucoside, Loliolide-β-d-glucopyranoside from Flue-cured Tobacco. Agricultural and Biological Chemistry: Vol. 46, No. 5, pp. 1409-1411.

7 citations






01 Jan 1982
TL;DR: In this paper, natural product structures are constructed using Irazunolide Experimental and Structure Solution and Refinement (SRS) techniques. But the authors do not discuss the relationship between the two steps.
Abstract: ............................................................................................................ x Chapter 1 Data Collection ....................................................................... 1 Chapter 2 Natural Product Structures ........................................... 8 A. Irazunolide Experimental ..................................................................... 12 Structure Solution and Refinement .................................... 13 Discussion ................................................................................ 21