Back to Search
Start Over
Allylation and Alkylation of Biologically Relevant Nucleophiles by Diallyl Sulfides
- Source :
- The Journal of Organic Chemistry. 82:776-780
- Publication Year :
- 2016
- Publisher :
- American Chemical Society (ACS), 2016.
-
Abstract
- Allyl sulfides are bioactive phytochemicals found in garlic, onion, and other members of the genus Allium. Here we showed that diallyl disulfide and diallyl trisulfide can transfer allyl side chains to low molecular weight thiols. Diallyl monosulfide is inert with respect to this allyl transfer reaction. On the other hand, diallyl sulfone, a known metabolite of diallyl monosulfide, alkylates both amines and thiols under physiologically relevant conditions via isomerization to an electrophilic vinyl sulfone.
- Subjects :
- Alkylation
Molecular Structure
010405 organic chemistry
Diallyl disulfide
organic chemicals
Metabolite
Organic Chemistry
food and beverages
Sulfides
010402 general chemistry
01 natural sciences
Allium
0104 chemical sciences
Allyl Compounds
chemistry.chemical_compound
Diallyl trisulfide
Nucleophile
chemistry
Electrophile
Organic chemistry
Disulfides
Allyl Sulfide
Isomerization
Subjects
Details
- ISSN :
- 15206904 and 00223263
- Volume :
- 82
- Database :
- OpenAIRE
- Journal :
- The Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....9089de14d4564c30a3abc6e5aab36dae
- Full Text :
- https://doi.org/10.1021/acs.joc.6b02517