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dehydrogenation of c terpinene in a ball mill

Solvent-free dehydrogenation of c-terpinene in a ball mill ...

2021.11.20  The present article reports on the solvent-free dehydrogenation of g-terpinene (1) in a planetary ball mill affording p-cymene (2) as the predominant

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Solvent-free dehydrogenation of ??-terpinene in a ball mill ...

2010.7.1  The present article reports on the solvent-free dehydrogenation of γ-terpinene (1) in a planetary ball mill affording p-cymene (2) as the predominant reaction

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Solvent-free dehydrogenation of γ-terpinene in a ball mill ...

2010.7.1  The present article reports on the solvent-free dehydrogenation of γ-terpinene (1) in a planetary ball mill affording p-cymene (2) as the predominant reaction

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Electronic Supporting Information Solvent-free Dehydrogenation

Figure S1: Influence of the water as auxiliary on the solvent-free oxidative dehydrogenation of γ-terpinene (1, 2 mmol) to p-cymene (2) with KMnO4 as oxidant (6 mmol, 3.8 g

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Sci-Hub Solvent-free dehydrogenation of γ-terpinene in a ball

Solvent-free dehydrogenation of γ-terpinene in a ball mill: investigation of reaction parameters. Green Chemistry, 12(7), 1288. doi:10.1039/c002819c

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sbm dehydrogenation of c terpinene in a ball mill.md - GitLab

sbm dehydrogenation of c terpinene in... Find file Blame History Permalink VI ca1ab5f1 dihog authored Oct 26, 2022. ca1ab5f1 ...

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The aromatisation of terpenes and steroids by dehydrogenation

2015.4.1  The present article reports on the solvent-free dehydrogenation of γ-terpinene (1) in a planetary ball mill affording p-cymene (2) as the predominant reaction

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Continuous catalyst-free aromatization of γ-terpinene

Abstract. The dehydrogenation of γ-terpinene was studied under catalyst- and solvent-free reaction conditions using air as an oxidant. The dehydrogenation affords p -cymene in good yields in a continuous flow

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Organic reactions of sulfur dioxide. Reactions with nucleophilic

Solvent-free dehydrogenation of γ-terpinene in a ball mill: investigation of reaction parameters. Green Chemistry 2010, 12 (7) , 1288. doi/10.1039/c002819c;

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