Sceletium (aizoaceae) alkaloids: total synthesis of racemic mesembranone, joubertinamine and epijoubertinamine☆☆☆
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[1] S. Takano,et al. Enantioselective synthesis of natural mesembrine using (D)-mannitol as a chiral template, a model study for the enantioselective synthesis of the amaryllidaceae alkaloids , 1982 .
[2] R. Webb,et al. Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine , 1982 .
[3] C. DeBoer,et al. Vapor-phase introduction of vinyl ketones in Michael additions , 1974 .
[4] C. Smith,et al. Centrally Active 2-(Substituted phenyl)-β-alanines1 , 1961 .
[5] E. R. Shepard,et al. Preparation of Some Homologs of Papaverine , 1950 .
[6] C. Murakata,et al. Chiral Route to Some Alkaloids through Asymmetric Iodolactonization , 1981 .
[7] K. Psotta,et al. The total synthesis of joubertinamine , 1979 .
[8] S. Martin,et al. New methods for alkaloid synthesis. Facile total syntheses of (.+-.)-O-methyljoubertiamine and (.+-.)-mesembrine , 1979 .
[9] U. Ghatak,et al. Investigation on the Sodium—Liquid Ammonia Cleavage of a Tosyl Protecting Group of Tosylamino Acids and Peptides1 , 1966 .