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A Total Synthesis of (±)-3‑O‑Demethylmacronine through Rearrangement of a Precursor Embodying the Haemanthidine Alkaloid Framework

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Figshare2017-03-31 更新2026-04-29 收录
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https://figshare.com/articles/dataset/A_Total_Synthesis_of_-3_i_O_i_Demethylmacronine_through_Rearrangement_of_a_Precursor_Embodying_the_Haemanthidine_Alkaloid_Framework/4809982
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A total synthesis of the racemic modification, (±)-2, of the tazettine-type alkaloid 3-O-demethyl­macronine is described. The key steps are an intramolecular Alder-ene (IMAE) reaction and a lactam-to-lactone rearrangement of tetracycle 13, a compound that embodies the haemanthidine alkaloid framework.
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2017-03-31
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