Abstract
A general method to synthesize various alphabeta alphabeta bis-strapped porphyrins, with a different functionalization on each side of the macrocycle, is described. The resulting new chelates may find applications as analogues of heme protein active sites, bifunctional chelates, or specific bis-chelating molecules with potential medical utility.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Binding Sites
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Chelating Agents / chemical synthesis*
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Chelating Agents / chemistry
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Hemeproteins / drug effects
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Metalloporphyrins / chemical synthesis*
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Metalloporphyrins / chemistry
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Models, Molecular
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Molecular Structure
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Stereoisomerism
Substances
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Chelating Agents
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Hemeproteins
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Metalloporphyrins