Synthesis of meso-substituted dihydro-1,3-oxazinoporphyrins

Scholarly Works

• Oleszak, C.; Schol, P. R.; Ritterhoff, C. L.; Krug, M.; Martin, M. M.; Bo, Y.; Meyer, B.; Clark, T.; Guldi, D. M.; Jux, N. Fused Hexabenzocoronene-Porphyrin Conjugates with Tailorable Excited-State Lifetimes. Angewandte Chemie (International ed. in English) 2024, 63, e202409363. doi:10.1002/anie.202409363
• Oleszak, C.; Schol, P. R.; Ritterhoff, C. L.; Krug, M.; Martin, M. M.; Bo, Y.; Meyer, B.; Clark, T.; Guldi, D. M.; Jux, N. Fused Hexabenzocoronene‐Porphyrin Conjugates with Tailorable Excited‐State Lifetimes. Angewandte Chemie 2024, 136. doi:10.1002/ange.202409363
• Sanusi, K.; Olukoya, A. O.; Sanyaolu, N. O.; Ibikunle, A. A.; Yussuf, S. T.; Ogundare, S. A.; Fatomi, N. O.; Atewolara-Odule, O. C.; Khoza, P. B. The Performance Evaluation of Meso-Tetraphenyl Porphyrin and Azo Dyes as Photosensitizers in Dye-sensitized Solar Cells. Journal of fluorescence 2024. doi:10.1007/s10895-024-03632-w
• Bastos, E. L.; Quina, F. H.; Baptista, M. S. Endogenous Photosensitizers in Human Skin. Chemical reviews 2023, 123, 9720–9785. doi:10.1021/acs.chemrev.2c00787
• Slitikov, P. V.; Evdokimenkova, Y. B. Aminomethylated Hydroxinaphthalenes: Synthesis and Application. Herald of the Bauman Moscow State Technical University. Series Natural Sciences 2021, 126–143. doi:10.18698/1812-3368-2021-1-126-143
• Ankit, L.; Bijoy, P. M.; Mahendra, N. Syntheses, Biological and Material Significance of Dihydro[1,3]oxazine Derivatives: An Overview. Current Organic Chemistry 2021, 25, 133–174. doi:10.2174/1385272824999201008154659
• Auras, B. L.; Oliveira, V. A.; Terenzi, H.; Neves, A.; Iglesias, B. A. meso-Mono-[4-(1,4,7-triazacyclononanyl)]-tri(phenyl)]porphyrin and the respective zinc(ii)-complex: complete characterization and biomolecules binding abilities. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 2016, 15, 564–579. doi:10.1039/c6pp00016a
• Singh, D. K.; Nath, M. Synthesis and spectroscopic properties of β-triazoloporphyrin-xanthone dyads. Beilstein journal of organic chemistry 2015, 11, 1434–1440. doi:10.3762/bjoc.11.155
• Figliola, C.; Male, L.; Horswell, S. L.; Grainger, R. S. N-Derivatives of peri-Substituted Dichalcogenide [FeFe]-Hydrogenase Mimics: Towards Photocatalytic Dyads for Hydrogen Production. European Journal of Inorganic Chemistry 2015, 2015, 3146–3156. doi:10.1002/ejic.201500355
• Karimipour, G.; Kowkabi, S.; Naghiha, A. New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity. Brazilian Archives of Biology and Technology 2015, 58, 431–442. doi:10.1590/s1516-8913201500024
• Singh, D. K.; Nath, M. Ambient temperature synthesis of β,β′-fused nickel(II) pyrrolo[1,2-a]pyrazinoporphyrins via a DBSA-catalyzed Pictet–Spengler approach. Organic & biomolecular chemistry 2015, 13, 1836–1845. doi:10.1039/c4ob02370f
• Nifant'ev, E. E.; Slitikov, P. V.; Rasadkina, E. N. Aminomethylated derivatives of 2,7-dihydroxynaphthalene. Doklady Chemistry 2014, 457, 129–131. doi:10.1134/s0012500814070052
• Singh, D. K.; Nath, M. First synthesis of meso-substituted pyrrolo[1,2-a]quinoxalinoporphyrins. Beilstein journal of organic chemistry 2014, 10, 808–813. doi:10.3762/bjoc.10.76

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