Facile Synthesis of a Benzindenoazepine Alkaloid, Bulgaramine, via Samarium Diiodide Promoted Ring Expansion of an α-Aminocarbonyl Compound
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo 142-8501, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol9004239
Reference31 articles.
1. aBlasko, G.InThe Alkaloids;Brossi, A., Ed.Academic Press Inc.:New York, 1990; pp157−224.
2. bLee, T. B.Illustrated Flora of Korea;Hanygmoonsa:Seoul, 1989; p385.
3. Aryl-radical cyclization onto an enamide double bond. A route to benz[d]indeno[l2-b]azepines
4. A new class of isoquinoline alkaloids: The indenobenzazepines
5. An efficient conversion of berberine into a rhoeadine via an indenobenzazepine
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