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  2. Diallyl disulfide - Wikipedia

    en.wikipedia.org/wiki/Diallyl_disulfide

    Diallyl disulfide and the related trisulfide are produced by decomposition of allicin, which is released upon breaking the cells of the Alliaceae plants, especially garlic. The diallyl disulfide yield is the highest for the steam distillation of garlic bulbs which contain about 2 wt.% of diallyl disulfide-rich oil. Diallyl disulfide can also be ...

  3. Category:Organic disulfides - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_disulfides

    Download as PDF; Printable version; In other projects ... General structure of a disulfide. Organic disulfides are chemical ... Diallyl disulfide;

  4. File:Diallyl-disulfide-from-xtal-3D-bs.png - Wikipedia

    en.wikipedia.org/wiki/File:Diallyl-disulfide...

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  5. File:Diallyl disulfide.svg - Wikipedia

    en.wikipedia.org/wiki/File:Diallyl_disulfide.svg

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  6. Diallyl trisulfide - Wikipedia

    en.wikipedia.org/wiki/Diallyl_trisulfide

    Diallyl trisulfide (DATS), also known as Allitridin, is an organosulfur compound with the formula S(SCH 2 CH=CH 2) 2. It is one of several compounds produced by hydrolysis of allicin , including diallyl disulfide and diallyl tetrasulfide; DATS is one of the most potent.

  7. File:1,2-diallyldisulfane 200.svg - Wikipedia

    en.wikipedia.org/wiki/File:1,2-diallyldisulfane...

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  8. Thiosulfinate - Wikipedia

    en.wikipedia.org/wiki/Thiosulfinate

    Methyl methanethiosulfinate can also disproportionate to a 1:1 mixture of dimethyl disulfide and methyl methanethiosulfonate (CH 3 SO 2 SCH 3) and rearrange via a Pummerer rearrangement to CH 3 S(O)CH 2 SSCH 3. [20] [21] An unusual three-membered ring thiosulfinate (a dithiirane 1-oxide) has been prepared through rearrangement of a 1,3 ...

  9. Allyl glycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Allyl_glycidyl_ether

    Most routes yield a racemic mixture. Epoxidation using monooxygenase enzyme proceeds enantioselectively. [8] The enantioselective synthesis of allyl glycidyl ether by microbial epoxidation of diallyl ether. Alternately, nucleophilic cyclization of either chirality of the secondary alcohol onto a primary tosylate gives the chiral epoxide product ...