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• W2123721958 startingPage "6595" @default.
• W2123721958 abstract "The enantiomerically pure chlorins 19 and 21 were synthesised from tripyrrolic nickel complex rac-17 and pyrrole building blocks 12 and 16. The pyrroles are annelated with norbornane moieties which contain the chiral information as well as two different functionalities. The functional groups, namely a carboxylic acid ester and a carbonitrile group, of chlorin 21 finally allowed the formation of an amino acid functionality at the periphery of the macrotetracycle. By using principles of peptide chemistry, the two chlorin subunits were joined to form the peptide-linked chlorin–chlorin dyad 24, which mimics the molecular parts of the natural photosynthetic reaction centre." @default.
• W2123721958 created "2016-06-24" @default.
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• W2123721958 date "2007-08-06" @default.
• W2123721958 modified "2023-10-17" @default.
• W2123721958 title "Synthesis of a Peptide-Linked Chlorin Dyad as a Model Compound for the Photosynthetic Reaction Centre" @default.
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• W2123721958 doi "https://doi.org/10.1002/chem.200700222" @default.
• W2123721958 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17516607" @default.
• W2123721958 hasPublicationYear "2007" @default.
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