Organic Letters 2001-07-26

MacDonald [2 + 2]-type condensation with vicinal diketones: synthesis and properties of novel spiro-tricyclic porphodimethenes.

M Harmjanz, I Bozidarević, M J Scott

Index: Org. Lett. 3(15) , 2281-4, (2001)

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Abstract

[structure: see text] Acid-catalyzed [2 + 2] condensation reactions of polycyclic aromatic vicinal diketones including aceanthrenequinone, phenathrenequinone, and pyrene-4,5-dione with 5-mesityldipyrromethanes are outlined, and this methodology provides a flexible entry to spiro-tricyclic porphodimethenes. The porphodimethene products have been fully characterized, including X-ray structure analyses and fluorescence spectroscopy. In the case of the phenanthrenone-substituted macrocycle, the two spiro-locks can be ring-opened to form a trans-bis(2'-hydroxymethylbiphenyl)-substituted porphyrin.

Related Compounds

  • 1,2-aceanthrylened...

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