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• W2912335063 abstract "A concise route toward two advanced fragments in the context of the total synthesis of the unique natural product azamerone is reported. Key synthetic features include the enantioselective synthesis of an epoxysilane and its Lewis-acid-induced cyclization and the installation of the pyridazine ring via a formylation/condensation sequence. This route provides strategic insights into the chemistry of phthalazinediols, facilitating synthetic approaches toward this class of natural products." @default.
• W2912335063 created "2019-02-21" @default.
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• W2912335063 date "2019-01-25" @default.
• W2912335063 modified "2023-10-14" @default.
• W2912335063 title "Synthesis of Two Key Fragments of the Complex Polyhalogenated Marine Meroterpenoid Azamerone" @default.
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• W2912335063 doi "https://doi.org/10.1021/acs.orglett.9b00090" @default.
• W2912335063 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30681874" @default.
• W2912335063 hasPublicationYear "2019" @default.
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