Kim, HyeBanwell, MartinWillis, Anthony2015-12-100022-3263http://hdl.handle.net/1885/62022The title alkaloids, 1, 2, and 3 respectively, have been prepared in a convergent manner by two related routes. The superior one involves C-H functionalization of the relevant 5-methoxyindole at C-7 using Hartwig's protocol and thus forming the correspondKeywords: Amaryllidaceae alkaloids; C-H functionalization; Natural products; Single crystal X-ray analysis; Total synthesis; Alkaloids; Nitrogen compounds; X ray analysis; Metabolites; 2 methoxypratosine; Amaryllidaceae alkaloid; indole; lycoranine A; lycoranine B;Convergent total syntheses of the amaryllidaceae alkaloids lycoranine A, lycoranine B and 2-methoxypratosine201310.1021/jo40069872016-02-24