Synthesis of taurospongin A: a potent inhibitor of DNA polymerase and HIV reverse transcriptase, using pi-allyltricarbonyliron lactone complexes

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.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2002-08 (15), p.1624-1625
Hauptverfasser: Hollowood, Christopher J, Ley, Steven V, Yamanoi, Shigeo
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container_title Chemical communications (Cambridge, England)
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creator Hollowood, Christopher J
Ley, Steven V
Yamanoi, Shigeo
description 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.
doi_str_mv 10.1039/b204994p
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source MEDLINE; Royal Society of Chemistry Journals Archive (1841-2007); Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Alkynes - chemical synthesis
Animals
Enzyme Inhibitors - chemical synthesis
Esters - chemical synthesis
Indicators and Reagents
Iron Compounds
Lactones
Magnetic Resonance Spectroscopy
Nucleic Acid Synthesis Inhibitors
Porifera - chemistry
Reverse Transcriptase Inhibitors - chemical synthesis
title Synthesis of taurospongin A: a potent inhibitor of DNA polymerase and HIV reverse transcriptase, using pi-allyltricarbonyliron lactone complexes
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