Pure and Applied Chemistry

CrossRef Cited-by Linking

• Nieder Jana B., Stojković Emina A., Moffat Keith, Forest Katrina T., Lamparter Tilman, Bittl Robert, Kennis John T. M.: Pigment–Protein Interactions in Phytochromes Probed by Fluorescence Line Narrowing Spectroscopy. J. Phys. Chem. B 2013, 131122100628004. <http://dx.doi.org/10.1021/jp409110q>
• Toganoh Motoki, Gokulnath Sabapathi, Kawabe Yasunori, Furuta Hiroyuki: Synthesis and Reactivity of 5,10,15-Triaryl Doubly N-Confused Bilanes. Chemistry A European Journal 2012, 18, 4380. <http://dx.doi.org/10.1002/chem.201103034>
• Brückner Christian, Ogikubo Junichi, McCarthy Jason R., Akhigbe Joshua, Hyland Michael A., Daddario Pedro, Worlinsky Jill L., Zeller Matthias, Engle James T., Ziegler Christopher J., Ranaghan Matthew J., Sandberg Megan N., Birge Robert R.: meso-Arylporpholactones and their Reduction Products. J. Org. Chem. 2012, 77, 6480. <http://dx.doi.org/10.1021/jo300963m>
• Ogikubo Junichi, Meehan Eileen, Engle James T., Ziegler Christopher J., Brückner Christian: meso-Aryl-3-alkyl-2-oxachlorins. J. Org. Chem. 2012, 77, 6199. <http://dx.doi.org/10.1021/jo300964v>
• Soares Ana R. M., Taniguchi Masahiko, Chandrashaker Vanampally, Lindsey Jonathan S.: Primordial Oil Slick and the Formation of Hydrophobic Tetrapyrrole Macrocycles. Astrobiology 2012, 12, 1055. <http://dx.doi.org/10.1089/ast.2012.0857>
• Stępień Marcin, Sprutta Natasza, Latos-Grażyński Lechosław: Figure-Eight-Strukturen, Möbius-Bänder und mehr: Konformation und Aromatizität von Porphyrinoiden. Angew. Chem. 2011, 123, 4376. <http://dx.doi.org/10.1002/ange.201003353>
• Senge Mathias O.: Extrovertierte Verwirrung - Linus Pauling, Melvin Calvin und Porphyrinisomere. Angew. Chem. 2011, 123, 4360. <http://dx.doi.org/10.1002/ange.201003660>
• Stępień Marcin, Sprutta Natasza, Latos-Grażyński Lechosław: Figure Eights, Möbius Bands, and More: Conformation and Aromaticity of Porphyrinoids. Angew. Chem. Int. Ed. 2011, 50, 4288. <http://dx.doi.org/10.1002/anie.201003353>
• Senge Mathias O.: Extroverted Confusion-Linus Pauling, Melvin Calvin, and Porphyrin Isomers. Angew. Chem. Int. Ed. 2011, 50, 4272. <http://dx.doi.org/10.1002/anie.201003660>
• This Hervé: The green beans challenge. Anal Bioanal Chem 2011, 399, 157. <http://dx.doi.org/10.1007/s00216-010-4292-5>
• Eriksson Emma S. E., Eriksson Leif A.: Predictive power of long-range corrected functionals on the spectroscopic properties of tetrapyrrole derivatives for photodynamic therapy. Phys Chem Chem Phys 2011, 13, 7207. <http://dx.doi.org/10.1039/c0cp02792h>
• Mass Olga, Taniguchi Masahiko, Ptaszek Marcin, Springer Joseph W., Faries Kaitlyn M., Diers James R., Bocian David F., Holten Dewey, Lindsey Jonathan S.: Structural characteristics that make chlorophylls green: interplay of hydrocarbon skeleton and substituents. New J Chem 2011, 35, 76. <http://dx.doi.org/10.1039/c0nj00652a>
• Krayer Michael, Yang Eunkyung, Diers James R., Bocian David F., Holten Dewey, Lindsey Jonathan S.: De novo synthesis and photophysical characterization of annulated bacteriochlorins. Mimicking and extending the properties of bacteriochlorophylls. New J Chem 2011, 35, 587. <http://dx.doi.org/10.1039/c0nj00771d>
• Mass Olga, Pandithavidana Dinesh R., Ptaszek Marcin, Santiago Koraliz, Springer Joseph W., Jiao Jieying, Tang Qun, Kirmaier Christine, Bocian David F., Holten Dewey: De novo synthesis and properties of analogues of the self-assembling chlorosomal bacteriochlorophylls. NJC 2011, 35, 2671. <http://dx.doi.org/10.1039/c1nj20611g>
• Campbell WM, Dombroski GS, Sharma I, Partridge AC, Collettt MG: Photodynamic chlorophyll a metabolites, including phytoporphyrin (phylloerythrin), in the blood of photosensitive livestock: Overview and measurement. N Z Vet J 2010, 58, 146. <http://dx.doi.org/10.1080/00480169.2010.67517>
• Linnanto J.M., Korppi-Tommola J.E.I.: Modelling excitonic energy transfer in the photosynthetic unit of purple bacteria. Chemical Phys 2009, 357, 171. <http://dx.doi.org/10.1016/j.chemphys.2009.01.001>
• Uno Hidemitsu, Hashimoto Masakazu, Fujimoto Akiko: Synthesis and Properties of Benzene-Fused Diporphyrins with Various Metals. HETEROCYCLES 2009, 77, 887. <http://dx.doi.org/10.3987/COM-08-S(F)55>
• Linnanto Juha M., Korppi-Tommola Jouko E. I.: Investigation on chlorosomal antenna geometries: tube, lamella and spiral-type self-aggregates. Photosynth Res 2008, 96, 227. <http://dx.doi.org/10.1007/s11120-008-9304-3>
• de Oliveira Kleber T., Silva Artur M.S., Tomé Augusto C., Neves Maria G.P.M.S., Neri Cláudio R., Garcia Vinicius S., Serra Osvaldo A., Iamamoto Yassuko, Cavaleiro José A.S.: Synthesis of new amphiphilic chlorin derivatives from protoporphyrin-IX dimethyl ester. Tetrahedron 2008, 64, 8709. <http://dx.doi.org/10.1016/j.tet.2008.06.103>
• Granzhan A., Penzkofer A., Hauska G.: Photo-degradation of bacteriochlorophyll c in intact cells and extracts from Chlorobium tepidum. J Photochem Photobiol A Chem 2004, 165, 75. <http://dx.doi.org/10.1016/j.jphotochem.2004.03.001>
• Brunner H, Schellerer K.-M: New porphyrin platinum conjugates for the cytostatic and photodynamic tumor therapy. Inorg Chim Ada 2003, 350, 39. <http://dx.doi.org/10.1016/S0020-1693(02)01490-1>
• Oberhuber Michael, Kräutler Bernhard: Breakdown of Chlorophyll: Electrochemical Bilin Reduction Provides Synthetic Access to Fluorescent Chlorophyll Catabolites. Chem Eur J of Chem Bio 2002, 3, 104. <http://dx.doi.org/10.1002/1439-7633(20020104)3:1<104::AID-CBIC104>3.0.CO;2-R>
• Mühlecker Walter, Ongania Karl-Hans, Kräutler Bernhard, Matile Philippe, Hörtensteiner Stefan: Dem Chlorophyllabbau in Pflanzen auf der Spur – Konstitutionsaufklärung eines „fluoreszierenden” Chlorophyllkataboliten. Angew Chem 1997, 109, 401. <http://dx.doi.org/10.1002/ange.19971090424>
• Brunner H., Schellerer K.-M., Treittinger B.: Synthesis and in vitro testing of hematoporphyrin type ligands in platinum(II) complexes as potent cytostatic and phototoxic antitumor agents. Inorg Chim Ada 1997, 264, 67. <http://dx.doi.org/10.1016/S0020-1693(97)05593-X>
• Anglada Maria Carme, Farrera Joan-Anton, Ribó Josep M.: One-electron redox processes of the CuII chelate of 3,8,12,17-tetraethyl-2,7,13,18-tetramethylbilin-1,19-dione. Tetrahetron Lett 1997, 38, 669. <http://dx.doi.org/10.1016/S0040-4039(96)02388-X>
• Porra Robert J.: Recent Progress in Porphyrin and Chlorophyll Biosynthesis. Photchem Photbio 1997, 65, 492. <http://dx.doi.org/10.1111/j.1751-1097.1997.tb08596.x>
• Kilpeläinen Ilkka, Kaltia Seppo, Kuronen Pirjo, Hyvärinen Kristiina, Hynninen Paavo H.: Assignment of the1H and13C NMR spectra of 132(R)-methoxychlorophylla using the two-dimensional HMQC and HMBC techniques. Magn Reson Chem 1994, 32, 29. <http://dx.doi.org/10.1002/mrc.1260320107>
• Mühlecker Walter, Kräutler Bernhard, Ginsburg Samuel, Matile Philippe: Breakdown of Chlorophyll: A Tetrapyrrolic Chlorophyll Catabolite from Senescent Rape Leaves. Preliminary communication. HCA 1993, 76, 2976. <http://dx.doi.org/10.1002/hlca.19930760822>
• Seel Christian, Vögtle Fritz, Nieger Martin: Ein Dipyrrino-Cryptand — Synthese, Kristallstruktur, Metallkomplexierung. Chem Ber 1992, 125, 447. <http://dx.doi.org/10.1002/cber.19921250223>
• Zhou De-Ling, Walder Peristera, Scheffold Rolf, Walder Lorenz: SN2 or Electron Transfer?? A new technique discriminates the mechanisms of oxidative addition of alkyl halides to corrinato- and porphyrinatocobalt(I). HCA 1992, 75, 995. <http://dx.doi.org/10.1002/hlca.19920750403>
• Kräutler Bernhard, Jaun Bernhard, Bortlik Karlheinz, Schellenberg Maja, Matile Philippe: Zum Rätsel des Chlorophyllabbaus: Die Konstitution eines secoporphinoiden Kataboliten. Angew Chem 1991, 103, 1354. <http://dx.doi.org/10.1002/ange.19911031020>
• Hynninen Paavo H.: The synthetic utility and mechanisms of the hydrogen iodide isomerization and the oxo reaction in the modification of chlorophyll derivatives. Liebigs Ann Chem 1990, 1990, 835. <http://dx.doi.org/10.1002/jlac.1990199001157>
• Porra Robert J.: The assay of chlorophylls a and b converted to their respective magnesium-rhodochlorin derivatives by extraction from recalcitrant algal cells with aqueous alkaline methanol: Prevention of allomerization with reductants. Biochim Biophys Acta Bioenerg 1990, 1015, 493. <http://dx.doi.org/10.1016/0005-2728(90)90083-G>
• Schlabach Martin, Rumpel Helmut, Limbach Hans-Heinrich: Untersuchung der Tautomerie15N-markierter Hydroporphyrine durch dynamische NMR-Spektroskopie. Angew Chem 1989, 101, 84. <http://dx.doi.org/10.1002/ange.19891010126>
• Schlabach Martin, Rumpel Helmut, Limbach Hans-Heinrich: Investigation of the Tautomerism of15N-Labeled Hydroporphyrins by Dynamic NMR Spectroscopy. Angew Chem Int Ed Engl 1989, 28, 76. <http://dx.doi.org/10.1002/anie.198900761>
• Wehrle Bernd, Limbach Hans-heinrich: NMR study of environment modulated proton tautomerism in crystalline and amorphous phthalocyanine. Chemical Phys 1989, 136, 223. <http://dx.doi.org/10.1016/0301-0104(89)80049-7>
• Vogel Emanuel, Haas Wilhelm, Knipp Bernd, Lex Johann, Schmickler Hans: Tetraoxaporphyrin-Dikation. Angew Chem 1988, 100, 445. <http://dx.doi.org/10.1002/ange.19881000339>
• Vogel Emanuel, Haas Wilhelm, Knipp Bernd, Lex Johann, Schmickler Hans: Tetraoxaporphyrin Dication. Angew Chem Int Ed Engl 1988, 27, 406. <http://dx.doi.org/10.1002/anie.198804061>
• Grubmayr Karl, Wagner Ulrike Gabriella: Zur Chemie der Thioladdition an 2,3-Dihydro-3-ethylidendipyrrin-1(10H)-one—eine Modellstudie zur kovalenten Chromophor-Protein-Bindung in Biliproteiden. Monatsh Chem 1988, 119-119, 965. <http://dx.doi.org/10.1007/BF00810106>
• Pasquier Cécile, Gossauer Albert, Keller Walter, Kratky Christoph: Syntheses of bile pigments. Part 15. First unequivocal assignment of the absolute configuration of an urobilinoid bile pigment by X-ray diffraction analysis of its synthetic precursor. HCA 1987, 70, 2098. <http://dx.doi.org/10.1002/hlca.19870700815>
• Nomenclature Committee of IUB (NC-IUB) and IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Newsletter 1988. Eur J Biochem 1987, 170, 7. <http://dx.doi.org/10.1111/j.1432-1033.1987.tb13661.x>