Abstract
The synthesis of taurospongin A has been achieved using, as a key step, a pi-allyltricarbonyliron lactone complex to control a highly stereoselective addition of a methyl group to a carbonyl unit located in the side chain of the complex.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alkynes / chemical synthesis*
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Animals
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Enzyme Inhibitors / chemical synthesis*
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Esters / chemical synthesis*
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Indicators and Reagents
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Iron Compounds
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Lactones
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Magnetic Resonance Spectroscopy
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Nucleic Acid Synthesis Inhibitors*
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Porifera / chemistry*
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Reverse Transcriptase Inhibitors / chemical synthesis*
Substances
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Alkynes
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Enzyme Inhibitors
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Esters
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Indicators and Reagents
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Iron Compounds
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Lactones
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Nucleic Acid Synthesis Inhibitors
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Reverse Transcriptase Inhibitors
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taurospongin A