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- W4308722498 endingPage "1392" @default.
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- W4308722498 abstract "We report a theoretical study of the first silver-dependent enantiodivergent gold-catalysed reaction. The combination of a single chiral binuclear gold(I) chloride complex and silver perchlorate catalyses the asymmetric intramolecular hydroamination of alkenes and affords both enantiomers of the products by applying a simple solvent change from toluene to methanol. A gold-silver chloride adduct that occurs only in methanol appears to control the enantioinversion. If one gold atom coordinates and activates the alkene moiety, the other gold is included in an adduct with silver chloride, which coordinates a methanol solvent molecule and further interacts with the amine function. If the use of toluene implies free anions and affords (S)-enantiomer, methanol allows a proximal interaction with the amine, leads to an opposite stereodifferentiation of the two diastereomeric intermediates during the final protodeauration step and results in the (R)-enantiomer." @default.
- W4308722498 created "2022-11-15" @default.
- W4308722498 creator A5020199494 @default.
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- W4308722498 creator A5028330159 @default.
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- W4308722498 creator A5087496358 @default.
- W4308722498 date "2022-11-08" @default.
- W4308722498 modified "2023-10-16" @default.
- W4308722498 title "Silver Dependent Enantiodivergent Gold(I) Catalysed Asymmetric Intramolecular Hydroamination of Alkenes: A Theoretical Study" @default.
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