Utilization of a phosphazene base allows hitherto unreactive nitroaromatic compounds to condense with ethyl isocyanoacetate to give c-annelated pyrroles. On the other hand, 3-nitropyridine reacted under these conditions to give a novel tricyclic heterocycle 13 in modest yield.

Porphyrins with fused aromatic rings are under detailed investigation due to their unique spectroscopic properties. To gain more insights into the effects due to ring annealation on the porphyrin chromophore, a series of fluoranthoporphyrins have been synthesized. Reaction of 3-nitrofluoranthene with isocyanoacetate esters in the presence of a phosphazene base afforded good yields of the fluorantho[2,3-c]pyrrole esters 8. Cleavage of the ester moiety with KOH in ethylene glycol afforded the parent heterocycle 9, and this condensed with 2 equiv of acetoxymethylpyrroles 10 in refluxing acetic acid-2-propanol to afford tripyrranes 11. Following cleavage of the tert-butyl ester protective groups with TFA, "3 + 1" condensation with pyrrole dialdehyde 12 gave the fluoranthoporphyrins 13 in good overall yields. In addition, reaction of tripyrrane 11 with acenaphthopyrrole dialdehyde 16 gave the mixed acenaphthofluoranthoporphyrin 17 in excellent yields. A difluoranthoporphyrin 18 was also prepared via a "2 + 2" MacDonald condensation. Reaction of fluoranthopyrrole 8a with dimethoxymethane in the presence of p-toluenesulfonic acid gave the symmetrical dipyrrylmethane 19, and following ester saponification, this was condensed with a dipyrrylmethane dialdehyde to afford the adj-difluoranthoporphyrin 18. The UV--vis spectra for these fluoranthoporphyrins gave a series of three broadened absorptions in the Soret band region, although the Q-bands were little effected by ring fusion. The nickel(II), copper(II), and zinc chelates were more unusual, showing strong absorptions near 600 nm. Difluoranthoporphyrin 18 showed many of the same spectroscopic features, although the presence of two ring fusions gave rise to an increase in the spectroscopic shifts. The mixed system 17 gave spectra that showed larger red shifts due to the acenaphthylene unit combined with the features due to the fluoranthene rings. This work further demonstrates the utility of aromatic ring fusion in altering the properties of porphyrinoid systems.

Porphyrins with Exocyclic Rings. Part 16. Synthesis and Spectroscopic Characterization of Fluoranthoporphyrins, a New Class of Highly Conjugated Porphyrin Chromophores. -The title compounds (VIII) and (XI) are prepared in order to test the influence of fused aromatic rings on the absorptions behavior of porphyrins. The spectrum of (VIIIc) shows large red shift. -(LASH, TIMOTHY D.; WERNER, TONYA M.; THOMPSON, MICHELLE L.; MANLEY, JERAD M.; J. Org. Chem. 66 (2001) 9, 3152-3159; Dep. Chem., Ill. State Univ., Normal, IL 61790, USA; EN)

Synthesis of Novel Pyrrolic Compounds from Nitroarenes and Isocyanoacetates Using a Phosphazene Superbase. -In the presence of a phosphazene base, hitherto unreactive nitroarenes react with ethyl isocyanate (II) to give a variety of C-anellated pyrroles. -(LASH, TIMOTHY D.; THOMPSON, MICHELLE L.; WERNER, TONYA M.; SPENCE, JOHN D.; Synlett (2000) 2, 213-216; Dep. Chem., Ill. State Univ., Normal, IL 61790, USA; EN)