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Chemical communications (Cambridge, England), 2023-06, Vol.59 (45), p.6929-6932
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2023
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
The first Zn-ProPhenol catalyzed asymmetric inverse-electron-demand Diels-Alder reaction has been accomplished. This protocol was carried out by a dual-activation mode under mild conditions, allowing the preparation of various biologically important dihydropyrans in good yields with excellent stereoselectivities.
The first Zn-ProPhenol catalyzed asymmetric inverse-electron-demand Diels-Alder reaction of β,γ-unsaturated α-ketoamides with β,γ-unsaturated ketones has been accomplished.