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Sulfenic acid, 1-propenyl

When onion is cut or cmshed, ( )-5 -l-propenyl-L-cysteine sulfoxide (isoalliin) is converted into ( )-l-propene-l-sulfenic acid. Different from garlic, (Z)-thiopropanal S-oxide, a lachrymatory factor, is formed from the sulfenic acid by lachrymatory factor synthase (Figure 18.6). The remaining ( )-l-propene-l-sulfenic acid and methyl sulfenic acid produced from 5 -methyl-L-eysteine sulfoxide ean form methyl 1-pro-pene-thiosulfinate and 1-propenyl methane thiosulfinate that are further converted to sulfides such as 1-propenyl methyl disulfide and 1-prope-nyl methyl trisulfide. [Pg.422]

Even considering the difference in the amount of 5 -alk(en)yl-L-cysteine sulfoxide, the total amount of thiosulfinates produced from onion is significantly lower than that from garlic being approximately 0.01-0.035 mg/g-fresh weight (Table 18.2). The reason for this is because most of the ( )-l-propene-l-sulfenic acid produced from E)-S-1-propenyl-L-cysteine sulfoxide is converted into a lachrymatory factor, and not so much can be used for the production of thiosulfinates. [Pg.424]


See other pages where Sulfenic acid, 1-propenyl is mentioned: [Pg.82]    [Pg.82]    [Pg.140]    [Pg.21]    [Pg.64]    [Pg.3665]    [Pg.422]   
See also in sourсe #XX -- [ Pg.82 ]




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3- -2-propenyll

Propenylation

Sulfenate

Sulfenates

Sulfene

Sulfenes

Sulfenic acids

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