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  2. Crocetane - Wikipedia

    en.wikipedia.org/wiki/Crocetane

    Crocetane, or 2,6,11,15-tetramethylhexadecane, is an isoprenoid hydrocarbon compound. Unlike its isomer phytane, crocetane has a tail-to-tail linked isoprenoid skeleton. Crocetane has been detected in modern sediments and geological records as a biomarker, often associated with anaerobic methane oxidation .

  3. Phytane - Wikipedia

    en.wikipedia.org/wiki/Phytane

    [2] Phytane has many structural isomers. Among them, crocetane is a tail-to-tail linked isoprenoid and often co-elutes with phytane during gas chromatography (GC) due to its structural similarity. Phytane also has many stereoisomers because of its three stereo carbons, C-6, C-10 and C-14. Whereas pristane has two stereo carbons, C-6 and C-10.

  4. Phytofluene - Wikipedia

    en.wikipedia.org/wiki/Phytofluene

    Phytofluene is a colorless carotenoid found naturally in tomatoes and other vegetables. It is the second product of carotenoid biosynthesis. [2] It is formed from phytoene in a desaturation reaction leading to the formation of five conjugated double bonds. In the following step, addition of carbon-carbon conjugated double bonds leads to the ...

  5. Phytoene - Wikipedia

    en.wikipedia.org/wiki/Phytoene

    Phytoene (/ ˈfaɪtoʊiːn /) is a 40-carbon intermediate in the biosynthesis of carotenoids. [1] The synthesis of phytoene is the first committed step in the synthesis of carotenoids in plants. Phytoene is produced from two molecules of geranylgeranyl pyrophosphate (GGPP) by the action of the enzyme phytoene synthase. [2]

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  7. Lawesson's reagent - Wikipedia

    en.wikipedia.org/wiki/Lawesson's_reagent

    Lawesson's reagent (LR) is a chemical compound used in organic synthesis as a thiation agent. Lawesson's reagent was first made popular by Sven-Olov Lawesson, who did not, however, invent it. Lawesson's reagent was first made in 1956 during a systematic study of the reactions of arenes with P 4 S 10. [1]

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