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

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  4. Category:Organic disulfides - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_disulfides

    Download as PDF; Printable version; In other projects ... This category has the following 2 subcategories, out of 2 total. ... Diallyl disulfide;

  5. Thiosulfinate - Wikipedia

    en.wikipedia.org/wiki/Thiosulfinate

    Allicin, S-benzyl phenylmethanethiosulfinate, and related thiosulfinates show radical-trapping antioxidant activity associated with easy formation of sulfenic acids [12] The acyclic thiosulfinates from Allium and Brassica species possess antimicrobial, antiparasitic, antitumor and cysteine protease inhibitory activity while the natural 1,2-dithiolane-1-oxides are growth inhibitors.

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

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  7. 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.

  8. The reaction of an electrophile with 1,3,2,4-dithiadiphosphetane 2,4-disulfides is less common, but the reaction of an alkyl halide with a 1,3,2,4-dithiadiphosphetane 2,4-disulfide forms a new compound with a sulfur-carbon bond and a phosphorus-halide bond.

  9. 2,2'-Dipyridyldisulfide - Wikipedia

    en.wikipedia.org/wiki/2,2'-Dipyridyldisulfide

    Print/export Download as PDF; ... 2,2′-Dipyridyldisulfide, ... for example to oxidise free thiols to form disulfide bonds in proteins.

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