Sceletium (aizoaceae) alkaloids: total synthesis of racemic mesembranone, joubertinamine and epijoubertinamine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Total synthesis of Sceletium alkaloids (±)-joubertinamine, (±)-epijoubertinamine, (±)-tortuosamine and formal synthesis of (±)-mesembrine, (±)-N-formyltortuosamine;New Journal of Chemistry;2016
2. Consecutive sigmatropic rearrangements in the enantioselective total synthesis of (−)-joubertinamine and (−)-mesembrine;Tetrahedron;2009-04
3. Oxidative Friedel−Crafts Reaction and its Application to the Total Syntheses of Amaryllidaceae Alkaloids;The Journal of Organic Chemistry;2009-02-06
4. A New Approach to 2-(1-Alkylcyclohex-2-En-1-Yl) Phenols;Synthetic Communications;1992-09
5. Intramolecular cyclization of ω-primary amino electrophilic olefins to functionalized pyrrolidines and piperidines.;Tetrahedron Letters;1987-01
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