Synthesis of 3-substituted 2-azaanthraquinones and 1,3-disubstituted 2-azaanthraquinones using the Larock isoquinoline synthesis and a protonucleophile-induced ring closing procedure
Autor: | Van Aeken, Sam, Abbaspour Tehrani, Kourosch |
---|---|
Přispěvatelé: | Department of Bio-engineering Sciences, Organic Chemistry |
Jazyk: | angličtina |
Rok vydání: | 2008 |
Předmět: | |
Popis: | 2-Azaanthraquinones are well known for their cytotoxicity and are an important topic in cancer research. The synthestic route presented is based upon a Lewis acid catalyzed or protonucleophile induced ring closure starting from o-(1-alkynyl)napthaldehydes. This approach allows the specific incorporation of substituents on postion 1 and 3 of the isoquinoline ring by variation of the alkyne moiety and the protonucleophile. |
Databáze: | OpenAIRE |
Externí odkaz: |