Enantioselective synthesis of (−)-gephyrotoxine 223AB [(3R,5R,9R)-3-butyl-5-propyloctahydroindolizine]
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference9 articles.
1. The structure of gephyrotoxin (GTX) 223AB
2. Asymmetric synthesis III. Enantiospecific synthesis of the natural 3r, 5r, 9r (−) gephyrotoxin-223 AB
3. 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
4. Enantioselective ruthenium-mediated synthesis of (-)-indolizidine 223AB
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1. C-H Functionalization of Amino Alcohols by Osmium Tetroxide/NMO or TPAP/NMO: Protecting Group-Free Synthesis of Indolizidines (-)-223AB and 3-epi -(-)-223AB;European Journal of Organic Chemistry;2019-12-19
2. Cross-Coupling of Cyclopropanols: Concise Syntheses of Indolizidine 223AB and Congeners;Organic Letters;2014-11-25
3. Enantioselective Syntheses of 2,5-Disubstituted Pyrrolidines Based on Iridium-Catalyzed Allylic Aminations-Total Syntheses of Alkaloids from Amphibian Skins;Chemistry - A European Journal;2011-05-24
4. ChemInform Abstract: Enantioselective Synthesis of (-)-Gephyrotoxine 223 AB ((3R,5R,9R)-3- Butyl-5-propyloctahydroindolizine).;ChemInform;2010-08-20
5. A General Approach to 3-n-Butyl-5-alkylindolizidines: Total Synthesis of (−)-Indolizidine 195B;The Journal of Organic Chemistry;2007-10-19
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