Senepodine A, a novel C22N2 alkaloid from Lycopodium chinense
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. For reviews of the Lycopodium alkaloids, see: (a) Ayer, W. A.; Trifonov, L. S. In The Alkaloids; Cordell, G. A.; Brossi, A., Eds.; Academic Press: New York, 1994; Vol. 45, p. 233; (b) Ayer, W. A. Nat. Prod. Rep. 1991, 8, 455; (c) MacLean, D. B. In The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1985; Vol. 26, p. 241; (d) MacLean, D. B. In The Alkaloids; Manske, R. H. F., Ed.; Academic Press: New York, 1973; Vol. 14, p. 348; (e) MacLean, D. B. In The Alkaloids; Manske, R. H. F., Ed.; Academic Press: New York, 1968; Vol. 10, p. 305.
2. Tandem Radical Cyclizations Initiated with α-Carbonyl Radicals: First Total Synthesis of (+)-Paniculatine
3. Total Synthesis of the Lycopodium Alkaloids Magellanine and Magellaninone by Three-fold Annulation of 2-Cyclopentenone
4. A Classical Paradigm of Alkaloid Biogenesis Revisited: Acetonedicarboxylic Acid as a Biosynthetic Precursor of Lycopodine
5. Biosynthesis of lycopodine: incorporation of acetate via an intermediate with C2v symmetry
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