Allylation and Alkylation of Biologically Relevant Nucleophiles by Diallyl Sulfides
Author:
Affiliation:
1. Department of Chemistry, University of Missouri, 125 Chemistry Building, Missouri 65211, United States
2. Department of Biochemistry, University of Missouri, 125 Chemistry Building, Columbia, Missouri 65211, United States
Funder
National Cancer Institute
National Center for Complementary and Alternative Medicine
Office of Dietary Supplements
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02517
Reference39 articles.
1. The Organosulfur Chemistry of the GenusAllium - Implications for the Organic Chemistry of Sulfur
2. Polysulfides as biologically active ingredients of garlic
3. Inhibition of cytochrome P-450 2E1 by diallyl sulfide and its metabolites
4. Comparative effects of mono-, di-, tri-, and tetrasulfides derived from plants of the Allium family: redox cycling in vitro and hemolytic activity and Phase 2 enzyme induction in vivo
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