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• W2003704341 abstract "Three different approaches toward the synthesis of the macrocyclic thiolactone core of griseoviridin have been studied. Intramolecular palladium-catalyzed thiol coupling and esterification (carboxylate activation) have led to the formation of unexpected rearranged products. An intermolecular palladium-catalyzed thiol/vinyl iodide coupling followed by an esterification (alcohol activation) ultimately led to the nine-membered core of griseoviridin." @default.
• W2003704341 created "2016-06-24" @default.
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• W2003704341 date "2003-06-01" @default.
• W2003704341 modified "2023-09-25" @default.
• W2003704341 title "Approaches toward the Total Synthesis of the Nine-Membered Thio-Lactone Core of Griseoviridin" @default.
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• W2003704341 doi "https://doi.org/10.1021/jo034195f" @default.
• W2003704341 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12816497" @default.
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