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

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

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  5. Inverse vulcanization - Wikipedia

    en.wikipedia.org/wiki/Inverse_vulcanization

    Poly (sulfur-random-diallyl disulfide) 2016: University of the Basque Country [20] 616 mA⋅h/g after 200cycles (at 0.2 C) Poly (sulfur-random-bismaleimide-divinylbenzene) 2016: Istanbul Technical University [21] 400 mA⋅h/g after 50 cycles (at 0.1 C) Poly (sulfur-random-styrene) 2017: University of Arizona [6] 485 mA⋅h/g after 1000 cycles ...

  6. 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 ...

  7. Category:Organic disulfides - Wikipedia

    en.wikipedia.org/wiki/Category:Organic_disulfides

    General structure of a disulfide Organic disulfides are chemical compounds with the general structure RSSR'. Wikimedia Commons has media related to Organic disulfides .

  8. Wikipedia:Reference desk/Archives/Science/2021 January 1 ...

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  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 ...