Unusual phlorins from the oxidative coupling of pentapyrromethanes: their facile conversion to meso-substituted porphyrins
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Oxidation of N21,N22-etheno-bridged 5H-phlorins to the monocationic N21, N22-etheno-bridged 5-alkylporphyrins by Cu(Bf4)2.
2. Regio- and stereoselective reduction of N(21),N(22)-bridged porphyrin hydroperchlorates to stable 5H-phlorins
3. Reduction of N-arylporphyrins to N-arylphlorins: opposite stereochemical courses as a function of the reducing agent
4. New routes from porphyrins to stable phlorins. Meso-alkylation and reduction of meso-tetraphenyl- and octaalkylporphyrins
5. Porphyrinogens and porphodimethenes, intermediates in the synthesis ofmeso-tetraphenylporphins from pyrroles and benzaldehyde
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4. Fluoride ion promoted NH deprotonation of dioxaPhlorin with NIR absorption vs. acid induced facile conversion to aromatic dioxaSapphyrin: Synthesis, spectroscopic and theoretical characterization;Journal of Porphyrins and Phthalocyanines;2021-05
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