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- W2024965575 abstract "Abstract The application of allylic sulphoxides and, particularly, the chiral amine reagent tert-butanesulphinamide has been extended to three different tandem processes. The condensation of (R)-(+)-allyl p-tolyl sulphoxide, fluorinated nitriles and alkyl propiolates led to a new family of enantiomerically pure fluorine-containing 1,4- dihydropyridines. A diastereoselective nucleophilic addition of fluorinated nucleophiles onto (R)-(tert-butanesulphinyl) imines, followed by an intramolecular aza-Michael reaction gave rise to either fluorinated isoindolines or 3-substituted indanones in a stereoselective manner." @default.
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- W2024965575 date "2013-04-01" @default.
- W2024965575 modified "2023-09-25" @default.
- W2024965575 title "Asymmetric Tandem Reactions: New Strategies and Applications" @default.
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- W2024965575 doi "https://doi.org/10.1080/10426507.2012.736105" @default.
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