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Allylation and Alkylation of Biologically Relevant Nucleophiles by Diallyl Sulfides

Authors :
Kasi Viswanatharaju Ruddraraju
Calvin D. Lewis
Kent S. Gates
Zachary D. Parsons
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.

Details

ISSN :
15206904 and 00223263
Volume :
82
Database :
OpenAIRE
Journal :
The Journal of Organic Chemistry
Accession number :
edsair.doi.dedup.....9089de14d4564c30a3abc6e5aab36dae