Highly Regioselective and Diastereoselective, One-Pot, Four-Component Synthesis of Novel Spiroindenoquinoxalineindolizidine Derivatives
Author:
Affiliation:
1. Department of Chemistry, Faculty of Sciences; Shahid Beheshti University; G. C., P.O. Box 1983963113 Tehran Iran
Publisher
Wiley
Subject
Organic Chemistry
Reference23 articles.
1. (-)-Indolizidine 167B via 4-Pyrrolylbutanals: Two Synthetic Methodologies at Comparison
2. Indolizidine and quinolizidine alkaloids
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1. Exo/endo stereocontrolled synthesis of spiroindoloindolizidines by using classical and microwave conditions via the 1,3‐dipolar cycloaddition reaction;Journal of Heterocyclic Chemistry;2020-05-20
2. Concise Synthesis of Tryptanthrin Spiro Analogues with In Vitro Antitumor Activity Based on One-Pot, Three-Component 1,3-Dipolar Cycloaddition of Azomethine Ylides to Сyclopropenes;Synthesis;2018-10-10
3. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones;Organic Chemistry Frontiers;2018
4. Chalcone: A Valuable Scaffold Upgrading by Green Methods;ACS Sustainable Chemistry & Engineering;2017-07-31
5. ChemInform Abstract: Highly Regioselective and Diastereoselective, One-Pot, Four-Component Synthesis of Novel Spiroindenoquinoxalineindolizidine Derivatives.;ChemInform;2015-08-20
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