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Abstract | Cited by

The first organocatalytic asymmetric assembly of Morita–Baylis–Hillman carbonates of isatins and α-angelica lactone has been studied, affording multifunctional products containing two valuable pharmacophores and vicinal quaternary chiral centers in high stereoselectivity (up to 92% ee, dr >95 : 5).

Graphical abstract: Asymmetric assembly of 2-oxindole and α-angelica lactone units to construct vicinal quaternary chiral centers

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