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- W2019798911 endingPage "10519" @default.
- W2019798911 startingPage "10515" @default.
- W2019798911 abstract "Abstract A sterically hindered homoenolate has been generated by the NHC‐catalyzed conjugate umpolung of β,β‐disubstituted enals and successfully employed in a facile stereoselective annulation with isatins. The strategy provides efficient access to spirocyclic oxindoles bearing two highly congested contiguous quaternary carbon centers. The use of a Brønsted acid cocatalyst was found to be crucial for guaranteeing both excellent reactivity and high stereoselectivity." @default.
- W2019798911 created "2016-06-24" @default.
- W2019798911 creator A5017167322 @default.
- W2019798911 creator A5034751002 @default.
- W2019798911 creator A5059479518 @default.
- W2019798911 creator A5077320577 @default.
- W2019798911 date "2014-08-14" @default.
- W2019798911 modified "2023-10-18" @default.
- W2019798911 title "Conjugate Umpolung of β,β-Disubstituted Enals by Dual Catalysis with an N-Heterocyclic Carbene and a Brønsted Acid: Facile Construction of Contiguous Quaternary Stereocenters" @default.
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