References analysis of the Wikipedia article "Porphyrin" in the English version

doi.org

Zhang, Wei; Lai, Wenzhen; Cao, Rui (2017). "Energy-Related Small Molecule Activation Reactions: Oxygen Reduction and Hydrogen and Oxygen Evolution Reactions Catalyzed by Porphyrin- and Corrole-Based Systems". Chemical Reviews. 117 (4): 3717–3797. doi:10.1021/acs.chemrev.6b00299. PMID 28222601.

Lash TD (2011). "Origin of aromatic character in porphyrinoid systems". Journal of Porphyrins and Phthalocyanines. 15 (11n12): 1093–1115. doi:10.1142/S1088424611004063.

Senge MO, MacGowan SA, O'Brien JM (December 2015). "Conformational control of cofactors in nature - the influence of protein-induced macrocycle distortion on the biological function of tetrapyrroles". Chemical Communications. 51 (96): 17031–17063. doi:10.1039/C5CC06254C. hdl:2262/75305. PMID 26482230.

Walker FA, Simonis U (2011). "Iron Porphyrin Chemistry". Encyclopedia of Inorganic and Bioinorganic Chemistry. doi:10.1002/9781119951438.eibc0104. ISBN 9781119951438.

Jentzen W, Ma JG, Shelnutt JA (February 1998). "Conservation of the conformation of the porphyrin macrocycle in hemoproteins". Biophysical Journal. 74 (2 Pt 1): 753–763. Bibcode:1998BpJ....74..753J. doi:10.1016/S0006-3495(98)74000-7. PMC 1302556. PMID 9533688.

Senge MO, Ryan AA, Letchford KA, MacGowan SA, Mielke T (2014). "Chlorophylls, Symmetry, Chirality, and Photosynthesis". Symmetry. 6 (3): 781–843. Bibcode:2014Symm....6..781S. doi:10.3390/sym6030781. hdl:2262/73843.

Zhang B, Lash TD (September 2003). "Total synthesis of the porphyrin mineral abelsonite and related petroporphyrins with five-membered exocyclic rings". Tetrahedron Letters. 44 (39): 7253. doi:10.1016/j.tetlet.2003.08.007.

Mason GM, Trudell LG, Branthaver JF (1989). "Review of the stratigraphic distribution and diagenetic history of abelsonite". Organic Geochemistry. 14 (6): 585. Bibcode:1989OrGeo..14..585M. doi:10.1016/0146-6380(89)90038-7.

Rothemund P (1936). "A New Porphyrin Synthesis. The Synthesis of Porphin". J. Am. Chem. Soc. 58 (4): 625–627. Bibcode:1936JAChS..58..625R. doi:10.1021/ja01295a027.

Rothemund P (1935). "Formation of Porphyrins from Pyrrole and Aldehydes". J. Am. Chem. Soc. 57 (10): 2010–2011. Bibcode:1935JAChS..57.2010R. doi:10.1021/ja01313a510.

Adler AD, Longo FR, Finarelli JD, Goldmacher J, Assour J, Korsakoff L (1967). "A simplified synthesis for meso-tetraphenylporphine". J. Org. Chem. 32 (2): 476. doi:10.1021/jo01288a053.

Wormald R, Evans J, Smeeth L, Henshaw K (July 2007). "Photodynamic therapy for neovascular age-related macular degeneration" (PDF). The Cochrane Database of Systematic Reviews (3): CD002030. doi:10.1002/14651858.CD002030.pub3. PMID 17636693.

Price M, Terlecky SR, Kessel D (2009). "A role for hydrogen peroxide in the pro-apoptotic effects of photodynamic therapy". Photochemistry and Photobiology. 85 (6): 1491–1496. doi:10.1111/j.1751-1097.2009.00589.x. PMC 2783742. PMID 19659920.

Singh S, Aggarwal A, Bhupathiraju NV, Arianna G, Tiwari K, Drain CM (September 2015). "Glycosylated Porphyrins, Phthalocyanines, and Other Porphyrinoids for Diagnostics and Therapeutics". Chemical Reviews. 115 (18): 10261–10306. doi:10.1021/acs.chemrev.5b00244. PMC 6011754. PMID 26317756.

Lewtak JP, Gryko DT (October 2012). "Synthesis of π-extended porphyrins via intramolecular oxidative coupling". Chemical Communications. 48 (81): 10069–10086. doi:10.1039/c2cc31279d. PMID 22649792.

Walter MG, Rudine AB, Wamser CC (2010). "Porphyrins and phthalocyanines in solar photovoltaic cells". Journal of Porphyrins and Phthalocyanines. 14 (9): 759–792. doi:10.1142/S1088424610002689.

Yella A, Lee HW, Tsao HN, Yi C, Chandiran AK, Nazeeruddin MK, et al. (November 2011). "Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency". Science. 334 (6056): 629–634. Bibcode:2011Sci...334..629Y. doi:10.1126/science.1209688. PMID 22053043. S2CID 28058582.

Alonso-Castro AJ, Zapata-Morales JR, Hernández-Munive A, Campos-Xolalpa N, Pérez-Gutiérrez S, Pérez-González C (May 2015). "Synthesis, antinociceptive and anti-inflammatory effects of porphyrins". Bioorganic & Medicinal Chemistry. 23 (10): 2529–2537. doi:10.1016/j.bmc.2015.03.043. PMID 25863493.

Bajju GD, Ahmed A, Devi G (December 2019). "Synthesis and bioactivity of oxovanadium(IV)tetra(4-methoxyphenyl)porphyrinsalicylates". BMC Chemistry. 13 (1): 15. doi:10.1186/s13065-019-0523-9. PMC 6661832. PMID 31384764.

Mendonça DA, Bakker M, Cruz-Oliveira C, Neves V, Jiménez MA, Defaus S, et al. (June 2021). "Penetrating the Blood-Brain Barrier with New Peptide-Porphyrin Conjugates Having anti-HIV Activity". Bioconjugate Chemistry. 32 (6): 1067–1077. doi:10.1021/acs.bioconjchem.1c00123. PMC 8485325. PMID 34033716.

Scott LJ, Goa KL (February 2000). "Verteporfin". Drugs & Aging. 16 (2): 139–146, discussion 146–8. doi:10.2165/00002512-200016020-00005. PMID 10755329. S2CID 260491296.

Vogel E, Köcher M (March 1986). "Porphycene—a Novel Porphin Isomer". Angewandte Chemie. 25 (3): 257. doi:10.1002/anie.198602571.

Nagamaiah J, Dutta A, Pati NN, Sahoo S, Soman R, Panda PK (March 2022). "3,6,13,16-Tetrapropylporphycene: Rational Synthesis, Complexation, and Halogenation". The Journal of Organic Chemistry. 87 (5): 2721–2729. doi:10.1021/acs.joc.1c02652. PMID 35061396. S2CID 246165814.

Dougherty TJ (2001). "Basic principles of photodynamic therapy". Journal of Porphyrins and Phthalocyanines. 5 (2): 105. doi:10.1002/jpp.328.

Vogel E, Guilard R (November 1993). "New Porphycene Ligands: Octaethyl- and Etioporphycene (OEPc and EtioPc)—Tetra- and Pentacoordinated Zinc Complexes of OEPc". Angewandte Chemie International Edition. 32 (11): 1600. doi:10.1002/anie.199316001.

Vogel E, Scholz P, Demuth R, Erben C, Bröring M, Schmickler H, et al. (October 1999). "Isoporphycene: The Fourth Constitutional Isomer of Porphyrin with an N(4) Core-Occurrence of E/Z Isomerism". Angewandte Chemie. 38 (19): 2919–2923. doi:10.1002/(SICI)1521-3773(19991004)38:19<2919::AID-ANIE2919>3.0.CO;2-W. PMID 10540393.

Hiroyuki F (1994). ""N-Confused Porphyrin": A New Isomer of Tetraphenylporphyrin". J. Am. Chem. Soc. 116 (2): 767. Bibcode:1994JAChS.116..767F. doi:10.1021/ja00081a047.

Chmielewski PJ, Latos-Grażyński L, Rachlewicz K, Glowiak T (18 April 1994). "Tetra-p-tolylporphyrin with an Inverted Pyrrole Ring: A Novel Isomer of Porphyrin". Angewandte Chemie International Edition. 33 (7): 779. doi:10.1002/anie.199407791.

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Rothemund P (1936). "A New Porphyrin Synthesis. The Synthesis of Porphin". J. Am. Chem. Soc. 58 (4): 625–627. Bibcode:1936JAChS..58..625R. doi:10.1021/ja01295a027.

Rothemund P (1935). "Formation of Porphyrins from Pyrrole and Aldehydes". J. Am. Chem. Soc. 57 (10): 2010–2011. Bibcode:1935JAChS..57.2010R. doi:10.1021/ja01313a510.

Hiroyuki F (1994). ""N-Confused Porphyrin": A New Isomer of Tetraphenylporphyrin". J. Am. Chem. Soc. 116 (2): 767. Bibcode:1994JAChS.116..767F. doi:10.1021/ja00081a047.

nih.gov

pubmed.ncbi.nlm.nih.gov

Scott LJ, Goa KL (February 2000). "Verteporfin". Drugs & Aging. 16 (2): 139–146, discussion 146–8. doi:10.2165/00002512-200016020-00005. PMID 10755329. S2CID 260491296.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

Scott LJ, Goa KL (February 2000). "Verteporfin". Drugs & Aging. 16 (2): 139–146, discussion 146–8. doi:10.2165/00002512-200016020-00005. PMID 10755329. S2CID 260491296.

Porphyrin (English Wikipedia)

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ncbi.nlm.nih.gov

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