
doi: 10.1007/128_2011_126
pmid: 21452079
Lycopodium alkaloids have attracted the attention of many natural product chemists and synthetic organic chemists due to their important biological activities and unique skeletal characteristics. In this review we describe isolation and asymmetric syntheses of several new alkaloids such as lycoposerramines-C, -V, -W, and cernuine, and show that asymmetric total synthesis played a key role in elucidating the structures of these complex natural products.
Biological Products, Alkaloids, Quinolizidines, Models, Chemical, Molecular Structure, Piperidines, Quinolines, Stereoisomerism, Heterocyclic Compounds, 4 or More Rings, Lycopodium
Biological Products, Alkaloids, Quinolizidines, Models, Chemical, Molecular Structure, Piperidines, Quinolines, Stereoisomerism, Heterocyclic Compounds, 4 or More Rings, Lycopodium
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