Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o -Formyl-β-nitrostyrenes

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Abstract

A highly diastereo- and enantioselective domino Michael/ Henry reaction of 1-acetylindolin-3-ones with o-formyl-(E)-β-nitrostyrenes catalyzed by low loading of a quinine-derived amine-squaramide provides the corresponding indolin-3-one derivatives bearing four adjacent stereogenic centers in good to high yields and with excellent stereoselectivities.

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Mahajan, S., Chauhan, P., Loh, C. C. J., Uzungelis, S., Raabe, G., & Enders, D. (2015). Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o -Formyl-β-nitrostyrenes. Synthesis (Germany), 47(7), 1024–1031. https://doi.org/10.1055/s-0034-1379943

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