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Palladium-catalyzed <i>ortho</i> -vinylation of β-naphthols with α-trifluoromethyl allyl carbonates: one-pot access to naphtho[2,1- <i>b</i> ]furans

Chiliveru Priyanka, Muppidi Subbarao, Nagender Punna

2021Organic & Biomolecular Chemistry14 citationsDOI

Abstract

Highly regio- and stereoselective ortho -vinylation of β-naphthols has been accomplished via CF 3 –π-allyl Pd-complex for the first time. Next, one-pot synthesis of CF 3 -naphtho[2,1- b ]furans is developed through a oxidative radical cyclization reaction.

Topics & Concepts

ChemistryPalladiumStereoselectivityCatalysisTrifluoromethylMedicinal chemistryOxidative phosphorylationOrganic chemistryAlkylBiochemistryFluorine in Organic ChemistryCatalytic C–H Functionalization MethodsCyclopropane Reaction Mechanisms
Palladium-catalyzed <i>ortho</i> -vinylation of β-naphthols with α-trifluoromethyl allyl carbonates: one-pot access to naphtho[2,1- <i>b</i> ]furans | Litcius