Stepwise Fusion of Porphyrin β,β′-Pyrrolic Positions to Imidazole Rings
Organic Letters2011Vol. 13(12), pp. 3110–3113
Citations Over Time
Abstract
A strategy for the stepwise annulation of pyrrolic rings of a porphyrin to imidazole rings is presented. Mono(imidazole), Janus and corner bis(imidazole), T-shaped tris(imidazole), and tetrakis(imidazole) porphyrins have been synthesized and characterized.
Related Papers
- → Synthesis of Natural Products, Carbocycles, and Heterocycles by Hauser–Kraus Annulation(2023)13 cited
- → [3 + 2] Annulation of Allylidenetriphenylphosphorane with 1,2-Diacylethylenes and 1,2-Diacylacetylenes: A One-Step Synthesis of Tri- and Tetrasubstituted Cyclopentadienes and Fulvenes(1997)38 cited
- → Stereocontrolled [4+1] Annulation of α‐Hydroxycyclobutenones: Synthesis of Polysubstituted Cyclopentenones(2016)7 cited
- → [4 + 2] Annulation of Activated o-Toluate/o-Tolualdehyde Donors (Hauser-Leusen Annulation)(2018)1 cited
- → [4 + 2] Annulation With Nonactivated o-Toluate Donors (Staunton-Weinreb-Myers Annulation)(2018)