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Desymmetrization Process by Mg(II)-Catalyzed Intramolecular Vinylogous Michael Reaction.

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Chiral magnesium catalyzed intramolecular vinylogous Michael reaction of novel cyclohexadienones via a desymmetrization process is reported. (R)-BINOL derived ligand and an achiral amide were employed in the current in situ… Click to show full abstract

Chiral magnesium catalyzed intramolecular vinylogous Michael reaction of novel cyclohexadienones via a desymmetrization process is reported. (R)-BINOL derived ligand and an achiral amide were employed in the current in situ generated magnesium catalyst, giving the corresponding hydrogenated benzofuranone skeletons in good to excellent enantioselectivities with high yields. This simple and efficient strategy could be utilized for the synthesis of aromatized α,β-unsaturated ester and Br-substituted hydrogenated benzofuranone in good yields under mild conditions.

Keywords: vinylogous michael; michael reaction; intramolecular vinylogous; desymmetrization process; catalyzed intramolecular

Journal Title: Organic letters
Year Published: 2020

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