Highly diastereoselective synthesis and NMR characterization of natural indolizidine alkaloids
Author:
Publisher
Wiley
Subject
Organic Chemistry
Reference8 articles.
1. Total synthesis of (+) monomorine I from chiral cyclic β-enamino ester
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3. Enantioselective synthesis of (5R,9R)-5-propyl-octahydroindolizine [(−)-gephyrotoxin 167B]
4. Enantioselective synthesis of (−)-gephyrotoxine 223AB [(3R,5R,9R)-3-butyl-5-propyloctahydroindolizine]
5. General entry to the 3,5-disubstituted indolizidine class of dendrobatid alkaloids. Total syntheses of both enantiomers of indolizidines 195B, 223AB, 239AB, and 239CD from a common chiral synthon
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1. Combined Chemical, Biological and Theoretical DFT-QTAIM Study of Potent Glycosidase Inhibitors Based on Quaternary Indolizinium Salts;European Journal of Organic Chemistry;2012-08-15
2. ChemInform Abstract: Highly Diastereoselective Synthesis and NMR Characterization of Natural Indolizidine Alkaloids.;ChemInform;2010-08-17
3. Concise syntheses of substituted indolizidine alkaloids via cyclization based on α-sulfinyl carbanions: preparation of (±)-indolizidines 167B and 209D, their epimers, and (±)-tashiromine;Tetrahedron;2008-03
4. Synthesis of alkylated indolizidine alkaloids via Pummerer mediated cyclization: synthesis of (±)-indolizidine 167B, (±)-5-butylindolizidine and (±)-monomorine I;Tetrahedron;2008-02
5. Bicyclic 5-6 Systems with One Bridgehead (Ring Junction) Nitrogen Atom: No Extra Heteroatom 0:0;Comprehensive Heterocyclic Chemistry III;2008
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