Concise Syntheses of the Cruciferous Phytoalexins Brassilexin, Sinalexin, Wasalexins, and Analogues: Expanding the Scope of the Vilsmeier Formylation
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
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0479866
Reference30 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. Unprecedented Vilsmeier Formylation: Expedient Syntheses of the Cruciferous Phytoalexins Sinalexin and Brassilexin and Discovery of a New Heteroaromatic Ring System
4. Biotransformation of the Brassica Phytoalexin Brassicanal A by the Blackleg Fungus
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