Portal de Periódicos da CAPES

Synthesis of Linear Tri‐ and Tetrapyrroles of Biogenetic Significance

1975; Wiley; Volume: 14; Issue: 6 Linguagem: Inglês

10.1002/anie.197504231

1521-3773

Burchard Franck, Arend Rowold,

Synthesis and Characterization of Pyrroles

Angewandte Chemie International Edition in EnglishVolume 14, Issue 6 p. 423-423 Communication Synthesis of Linear Tri- and Tetrapyrroles of Biogenetic Significance†‡ Prof. Dr. Burchard Franck, Corresponding Author Prof. Dr. Burchard Franck Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Search for more papers by this authorDr. Arend Rowold, Dr. Arend Rowold Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Search for more papers by this author Prof. Dr. Burchard Franck, Corresponding Author Prof. Dr. Burchard Franck Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Search for more papers by this authorDr. Arend Rowold, Dr. Arend Rowold Organisch-Chemisches Institut der Universität, 44 Münster, Orleans-Ring 23 (Germany)Search for more papers by this author First published: June 1975 https://doi.org/10.1002/anie.197504231Citations: 16 † Tetrapyrrole Biosynthesis, Part 3.—Part 2: B. Franck, D. Gantz, F.-P. Montforts, and F. Schmidtchen, Angew. Chem. 84, 433 (1972); Angew. Chem. internat. Edit. 11, 421 (1972). ‡ This work was supported by the Deutsche Forschungsgemeinschaft and the Fonds der Chemischen Industrie. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. References 1 Tetrapyrrole Biosynthesis, Part 3.—Part 2: B. Franck, D. Gantz, F.-P. Montforts, and F. Schmidtchen, Angew. Chem. 84, 433 (1972); Angew. Chem. internat. Edit. 11, 421 (1972). 2 G. H. Cookson and C. Rimington, Biochem. J. 57, 476 (1954). 3 Synthesis of a partially protected, similar tripyrrole and condensation experiments have recently also been reported by other authors: J. M. Osgerby, J. Pluscec, Y. C. Kim, F. Boyer, N. Stojanac, H. D. Mah, and S. F. MacDonald, Can. J. Chem. 50, 2652 (1972); R. B. Frydman, A. Valasinas, S. Levy, and B. Frydman, FEBS Lett. 38, 134 (1974). 4 G. P. Arsenault and S. F. MacDonald, Can. J. Chem. 39, 2043 (1961); B. Frydman, S. Reil, A. Valasinas, R. B. Frydman, and H. Rapoport, J. Amer. Chem. Soc. 93, 2738 (1971). 5 We are are grateful to Dr. U. Rapp, Varian MAT, Bremen, for the field-desorption mass spectra (FD-MS). 6 G. W. Kenner, K. M. Smith, and J. F. Unsworth, J. C. S. Chem. Comm. 1973, 43. 7 R. Radmer and L. Bogorad, Biochemistry 11, 904 (1972). 8 The resulting uroporphyrinogen mixtures were analyzed after dehydrogenation and decarboxylation to the coproporphyrins by G. Ufer (Diplomarbeit. Universität Münster 1974) by chromatography according to the method of P. R. Edmondson and S. Schwartz, J. Biol. Chem. 205, 605 (1953). Citing Literature Volume14, Issue6June 1975Pages 423-423 ReferencesRelatedInformation