Nucleophilic addition of lithio derivatives to 1-substituted benzo[c][2,7]naphthyridines (2,9-diazaphenanthrenes)
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1995/P1/P19950000979
Reference23 articles.
1. Directed Metalation of Pi-Deficient Azaaromatics: Strategies of Functionalization of Pyridines, Quinolines, and Diazines
2. A Simple Synthesis of Amphimedine
3. Marine pyridoacridine alkaloids: structure, synthesis, and biological chemistry
4. First metalation of aryl iodides: directed ortho-lithiation of iodopyridines, halogen-dance, and application to synthesis
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1. Functionalization of 4-bromobenzo[c][2,7]naphthyridine via regioselective direct ring metalation. A novel approach to analogues of pyridoacridine alkaloids;Beilstein Journal of Organic Chemistry;2019-09-26
2. Gold-catalyzed intramolecular cyclization/condensation sequence: synthesis of 1,2-dihydro[c][2,7]naphthyridines;Organic & Biomolecular Chemistry;2017
3. A novel approach to ring A analogues of the marine pyridoacridine alkaloid ascididemin;Tetrahedron;2013-11
4. Regioselective homolytic substitution of benzo[c][2,7]naphthyridines;Tetrahedron;2012-06
5. ChemInform Abstract: Nucleophilic Addition of Lithio Derivatives to 1-Substituted Benzo(c)( 2,7)naphthyridines (2,9-Diazaphenanthrenes).;ChemInform;2010-08-17
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