Radical cyclization of β-aminoacrylates: Stereoselective synthesis of indolizidines 167B and 209D
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Interaction of gephyrotoxin and indolizidine alkaloids with the nicotinic acetylcholine receptorion channel complex of torpedo electroplax
2. Enantioselective total syntheses of indolizidine alkaloids 167B and 209D
3. Short, enantiogenic syntheses of (-)-indolizidine 167B and (+)-monomorine
4. Enantioselective synthesis of (5R,9R)-5-propyl-octahydroindolizine [(−)-gephyrotoxin 167B]
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1. A Simple Entry to the 5,8-Disubstituted Indolizidine Skeleton via Hetero Diels-Alder Reaction;Molecules;2023-10-28
2. The Multi Steps Synthetic Methods of (±)-Indolizidine 209D as an Amphibian Natural Product in the Family of Alkaloids;The Natural Products Journal;2021-08
3. Recent applications of the Wittig reaction in alkaloid synthesis;The Alkaloids;2020
4. Silver-Catalyzed Decarboxylative Radical Azidation of Aliphatic Carboxylic Acids in Aqueous Solution;Journal of the American Chemical Society;2015-07-30
5. Total Synthesis of Indolizidine Alkaloids (-)-167B, (-)-209I, and (-)-223A by Using a Common Tricyclic Lactone;European Journal of Organic Chemistry;2015-02-09
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