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- W3100848550 abstract "The benzylic C–H group of α,α-dicyanoolefins from 3-substituted 1-indanones could be significantly activated via transmission along the aromatic system, thus enabling dynamic kinetic resolution via a traditional reversible deprotonation–protonation process. Enantioenriched 9-substituted 9H-fluorene frameworks were finally constructed through an asymmetric vinylogous Michael addition to nitroolefins, followed by a cascade cyclization and oxidative aromatization process, under the catalysis of a chiral bifunctional thiourea-tertiary amine." @default.
- W3100848550 created "2020-11-23" @default.
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- W3100848550 date "2020-11-11" @default.
- W3100848550 modified "2023-10-05" @default.
- W3100848550 title "Construction of Enantioenriched 9<i>H</i>-Fluorene Frameworks via a Cascade Reaction Involving Remote Vinylogous Dynamic Kinetic Resolution" @default.
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- W3100848550 doi "https://doi.org/10.1021/acs.orglett.0c03372" @default.
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