Summary
By means of copper catalyzed intramolecular coupling of the easily accessible 1,2-bis-(1-iodo-dipyrrin-9-yl)-ethanes and subsequent demetallation of the intermediate copper complexes corrphycenes could be prepared in nearly 40% overall yields.
Zusammenfassung
Durch Kupfer katalysierte intramolekulare Kupplung der leicht zugänglichen 1,2-bis-(1-Iod-dipyrrin-9-yl)-ethane und anschließende Demetallierung der gebildeten Kupferkomplexe ergibt Corrphycene in Gesamtausbeuten von fast 40%.
Similar content being viewed by others
References
Part XV: Chen Q-Q, Falk H (1995) Monatsh Chem126: 1323
Dolphin D (1979) The porphyrins. Academic Press, New York
Vogel E (1993) Pure Appl Chem65: 143
Sessler JL, Hemmi G, Mody Mit, 10. Mai 1995, Murai T, Burrell A, Young SW (1994) Acc Chem Res27: 43
Sessler JL, Brucker EA, Weghorn SJ, Kisters M, Schäfer M, Lex J, Vogel E (1994) Angew Chem106: 2402
McMurry JE (1989) Chem Rev89: 1513; Lenoir D (1989) Synthesis1989: 883 and references therein
For leading references see Falk H (1989) The chemistry of linear oligopyrroles and bile pigments. Springer, Wien New York
Chen Q-Q, Falk H (1995) Monatsh Chem126: 1233
Chen Q-Q, Falk H, Micura R (1995) Monatsh Chem126: 473
Paine III JB, Woodward RB, Dolphin D (1976) J Org Chem41, 2826
Fanta PE (1964) Chem Rev64: 613
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Falk, H., Chen, Q.Q. On the chemistry of pyrrole pigments, XCVI: An efficient synthesis of corrphycenes. Monatsh Chem 127, 69–75 (1996). https://doi.org/10.1007/BF00807410
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00807410