Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 46, Pages 4851-4853Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b714612d
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The repeated introduction of an a-dione unit and its reaction with an arene-1,2-diamine allows the stepwise annulation of all four pyrrolic rings of a porphyrin, as is demonstrated by the synthesis of a trisquinoxalinoporphyrin, a tetrakisquinoxalinoporphyrin and the more elaborated bisporphyrin.
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