Unprecedented Vilsmeier Formylation: Expedient Syntheses of the Cruciferous Phytoalexins Sinalexin and Brassilexin and Discovery of a New Heteroaromatic Ring System
Author:
Affiliation:
1. Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon SK, S7N 5C9 Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol015691y
Reference17 articles.
1. (a) Jones, G.; Stanforth, S. P. InOrganic Reactions; Paquette, L. A., Ed.; Wiley: New York, 1997; Vol. 49, pp 1−330.
2. Vilsmeier formylation and glyoxylation reactions of nucleophilic aromatic compounds using pyrophosphoryl chloride
3. Biotransformation of the Brassica Phytoalexin Brassicanal A by the Blackleg Fungus
4. Tyrosine Kinase Inhibitors. 4. Structure-Activity Relationships among N- and 3-Substituted 2,2'-Dithiobis(1H-indoles) for in vitro Inhibition of Receptor and Nonreceptor Protein Tyrosine Kinases
5. Phytoalexins from crucifers: synthesis, biosynthesis, and biotransformation
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