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- W4231650476 endingPage "3044" @default.
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- W4231650476 abstract "Abstract An unprecedented way to extend the synthetic utility of the Diels–Alder reaction to include a vinylogous reactivity space is described. A commercially available chiral phosphoric acid catalyst effectively activates cyclic 2,4‐dienones towards a vinylogous [4+2] cycloaddition with 2‐vinylindoles, which leads to stereochemically dense tetrahydrocarbazoles. The reaction proceeds with a high level of remote stereocontrol and exclusive chemoselectivity for the more distant double bond of the dienone." @default.
- W4231650476 created "2022-05-12" @default.
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- W4231650476 date "2014-02-06" @default.
- W4231650476 modified "2023-10-18" @default.
- W4231650476 title "Asymmetric Vinylogous Diels-Alder Reactions Catalyzed by a Chiral Phosphoric Acid" @default.
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- W4231650476 doi "https://doi.org/10.1002/ange.201310487" @default.
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