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Straightforward access to densely substituted chiral succinimides through enantioselective organocatalyzed Michael addition of α-alkyl-cyclic ketones to maleimides

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A simple organocatalytic system provides efficient access to a series of densely substituted chiral succinimides bearing a quaternary–tertiary carbon stereocenter sequence in good yields, with high diastereo- and enantioselectivities through… Click to show full abstract

A simple organocatalytic system provides efficient access to a series of densely substituted chiral succinimides bearing a quaternary–tertiary carbon stereocenter sequence in good yields, with high diastereo- and enantioselectivities through enantioselective conjugate addition of unreactive α-alkyl cyclic ketones to maleimides under microwave-assisted conditions.

Keywords: alkyl cyclic; ketones maleimides; substituted chiral; densely substituted; cyclic ketones; chiral succinimides

Journal Title: Organic chemistry frontiers
Year Published: 2020

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