Concise total syntheses of Marinoquinolines A–C
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Marinoquinolines A−F, Pyrroloquinolines from Ohtaekwangia kribbensis (Bacteroidetes)
2. Rapidithrix thailandica gen. nov., sp. nov., a marine gliding bacterium isolated from samples collected from the Andaman sea, along the southern coastline of Thailand
3. Palladium-Catalyzed, Modular Synthesis of Highly Functionalized Indoles and Tryptophans by Direct Annulation of Substituted o-Haloanilines and Aldehydes
4. A Flexible, Palladium-Catalyzed Indole and Azaindole Synthesis by Direct Annulation of Chloroanilines and Chloroaminopyridines with Ketones
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1. Three-Component Ring-Expansion Reaction of Indoles Leading to Synthesis of Pyrrolo[2,3-c]quinolines;Organic Letters;2023-09-07
2. Pictet-spengler/transamination cascade reaction of indoles for modular synthesis of marinoquinoline analogues;Green Synthesis and Catalysis;2023-09
3. Environmentally friendly domino multicomponent strategy for the synthesis of pyrroloquinolinone hybrid heterocycles;RSC Advances;2022
4. Bioactive natural products from Bacteroidetes;Natural Product Reports;2022
5. Methods for the synthesis of 3H-pyrrolo[2,3-c]quinolines;Chemistry of Heterocyclic Compounds;2021-12
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