Facile three-component domino reactions in the regioselective synthesis and antimycobacterial evaluation of novel indolizines and pyrrolo[2,1-a]isoquinolines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference50 articles.
1. Highly Enantioselective Approach to Indolizidines: Preparation of (+)-(1S,8aS)-1-Hydroxyindolizidine and (−)-Slaframine
2. Enantioselective Allyltitanation. Synthesis of (-)-Slaframine
3. Synthesis of Optically Active Indolizidines: (-)-8a-epi-Dendroprimine and (-)-7,8-Dehydro-5,6-dimethylindolizidine
4. Enantioselective synthesis of (−)-indolizidine 167B
5. A short and concise synthetic route to (−)-coniceine
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1. C-1 Substituted isoquinolines potentiate the antimycobacterial activity of rifampicin and ethambutol;Frontiers in Antibiotics;2023-05-09
2. A domino reaction for the synthesis of pyrrolo[2,1-a]isoquinolines from 2-aryl-pyrrolidines and alkynes promoted by a four-component catalytic system under aerobic conditions;RSC Advances;2023
3. Modification of Pyrrolo[2,1-a]isoquinolines and Polysubstituted Pyrroles via Methylenation with Acetyl Chloride and Dimethylsulfoxide;The Journal of Organic Chemistry;2022-08-11
4. Iron-Catalyzed Synthesis of Pyrrolo[2,1-a]isoquinolines via 1,3-Dipolar Cycloaddition/Elimination/Aromatization Cascade and Modifications;Synlett;2022-07-11
5. A Two-Step Approach to a Hexacyclic Lamellarin Core via 1,3-Dipolar Cycloaddition of Isoquinolinium Ylides to Nitrostilbenes;The Journal of Organic Chemistry;2022-04-25
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