Synthesis of the heterocyclic core of the alkaloids martinelline and martinellic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
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1. Synthesis of the Hexahydropyrrolo-[3,2-c]-quinoline Core Structure and Strategies for Further Elaboration to Martinelline, Martinellic Acid, Incargranine B, and Seneciobipyrrolidine;Molecules;2021-01-11
2. Construction of a (3aR,4R,9bR)-Hexahydropyrroloquinoline by Stereoselective Hydrogen-Mediated Domino Cyclization;Organic Process Research & Development;2019-02-20
3. Catalytic Enantioselective Synthesis of the Partially Reduced Tricyclic Pyrrolo[3,2-c]quinoline Core Structure of theMartinellaAlkaloids;ChemistrySelect;2016-06-01
4. Enantioselective Total Synthesis of (−)‐Martinellic Acid;Angewandte Chemie International Edition;2015-11-17
5. Enantioselective Total Synthesis of (−)‐Martinellic Acid;Angewandte Chemie;2015-11-17
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