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- W2152016557 endingPage "14149" @default.
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- W2152016557 abstract "The highly efficient synthesis of the enantioenriched spiroindolines by iridium-catalyzed asymmetric allylic dearomatization and reduction is presented. Spiroindolines containing three contiguous stereogenic centers were obtained with excellent diastereo- and enantioselectivity. In addition, a chiral tryptamine derivative could be easily accessed in good yield with excellent ee value through an unprecedented dearomatization/retro-Mannich/hydrolysis cascade reaction of an indole derivative." @default.
- W2152016557 created "2016-06-24" @default.
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- W2152016557 date "2015-09-25" @default.
- W2152016557 modified "2023-10-16" @default.
- W2152016557 title "Enantioselective Construction of Spiroindolines with Three Contiguous Stereogenic Centers and Chiral Tryptamine Derivatives via Reactive Spiroindolenine Intermediates" @default.
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- W2152016557 doi "https://doi.org/10.1002/anie.201507193" @default.
- W2152016557 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26403164" @default.
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