Mild Methodology for [4+1] Pyrroline Annulation. Second Generation Synthesis of Pyrrolizidine Alkaloids
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918708063965
Reference13 articles.
1. Fellow of the Alfred P. Sloan Foundation, 1981–85; Recipient of the National Institutes of Health Research Career Development Award, 1984–1989 (AI-00564)
2. Intramolecular [4 + 1] pyrroline annulation approach to pyrrolizidine alkaloids. Formal total synthesis of (±)-supinidine.
3. Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine
4. Rearrangements of a 2-vinylaziridine
5. Iodotrimethylsilane—a versatile synthetic reagent
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