Total Synthesis of Marinomycins A-C

Ocean's three: Unearthed from the bottom of the ocean off the coast of La Jolla (California, USA), marinomycins A–C, which differ in geometry about the C8C9 and C8′C9′ double bonds, have been prepared by total synthesis through a strategy that features a Suzuki coupling reaction to forge thei...

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Veröffentlicht in:Angewandte Chemie International Edition 2006-10, Vol.45 (39), p.6527-6532
Hauptverfasser: Nicolaou, K. C., Nold, Andrea L., Milburn, Robert R., Schindler, Corinna S.
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container_issue 39
container_start_page 6527
container_title Angewandte Chemie International Edition
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creator Nicolaou, K. C.
Nold, Andrea L.
Milburn, Robert R.
Schindler, Corinna S.
description Ocean's three: Unearthed from the bottom of the ocean off the coast of La Jolla (California, USA), marinomycins A–C, which differ in geometry about the C8C9 and C8′C9′ double bonds, have been prepared by total synthesis through a strategy that features a Suzuki coupling reaction to forge their remarkable polyunsaturated 44‐membered‐ring systems (see picture).
doi_str_mv 10.1002/anie.200601867
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Actinobacteria - chemistry
Alkenes - chemical synthesis
Anti-Bacterial Agents - chemical synthesis
antibiotics
Antibiotics, Antineoplastic - chemical synthesis
antitumor agents
Crystallography, X-Ray
Indicators and Reagents
Lactones - chemical synthesis
Macrolides - chemical synthesis
Magnetic Resonance Spectroscopy
Models, Molecular
natural products
Photochemistry
Stereoisomerism
Suzuki coupling
total synthesis
title Total Synthesis of Marinomycins A-C
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