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• W2893612812 abstract "A unified strategy for protecting-group-free synthesis of alkaloids lennoxamine, chilenine, fumaridine, 8-oxypseudoplamatine, and 2- O-(methyloxy)fagaronine is reported. The core isoindolin-1-one and isoquinolin-1-one structures were built by a silver-catalyzed regio- and stereoselective cyclization of methyl 2-alkynylbenzimidates. The regioselectivity of cyclization was achieved by utilizing the intrinsic functionality of alkaloids." @default.
• W2893612812 created "2018-10-05" @default.
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• W2893612812 date "2018-09-28" @default.
• W2893612812 modified "2023-09-24" @default.
• W2893612812 title "Regio- and Stereoselective Electrophilic Cyclization Approach for the Protecting-Group-Free Synthesis of Alkaloids Lennoxamine, Chilenine, Fumaridine, 8-Oxypseudoplamatine, and 2-<i>O</i>-(Methyloxy)fagaronine" @default.
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• W2893612812 doi "https://doi.org/10.1021/acs.joc.8b02154" @default.
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