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First Synthesis of Azachlorins and Azacorrins with a N-Atom in β-Pyrrolic Positions
Azachlorins 7 and 11, and azahexadehydrocorrin rac‐10 are novel structural types of tetrapyrrolic macrocycles. Synthesis of the target structures bearing N‐atoms in the β‐periphery of the macrotetracycles could be achieved by attaching an imidazole moiety 4 to the tricyclic Ni complex rac‐5, followe...
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Published in: | Helvetica chimica acta 2014-02, Vol.97 (2), p.188-196 |
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container_title | Helvetica chimica acta |
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creator | Vu, Nghiem Hai Damke, Jan-Erik Borrmann, Tobias Latos-Grażyński, Lechosław Montforts, Franz-Peter |
description | Azachlorins 7 and 11, and azahexadehydrocorrin rac‐10 are novel structural types of tetrapyrrolic macrocycles. Synthesis of the target structures bearing N‐atoms in the β‐periphery of the macrotetracycles could be achieved by attaching an imidazole moiety 4 to the tricyclic Ni complex rac‐5, followed by cyclization. Depending on the central metal ion of the bilin intermediates rac‐6a and rac‐6b, chlorin‐ or corrin‐type structures were formed by cyclization. |
doi_str_mv | 10.1002/hlca.201300303 |
format | article |
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source | Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list) |
subjects | Azabilin Azachlorin Azacorrin Tetrapyrroles |
title | First Synthesis of Azachlorins and Azacorrins with a N-Atom in β-Pyrrolic Positions |
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