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- W3209515934 endingPage "14926" @default.
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- W3209515934 abstract "The first chiral phosphoric acid (CPA) catalyzed cycloaddition-elimination cascade reaction of 2-naphthol- and phenol-derived enecarbamates with azonaphthalenes has been established, providing a highly atroposelective route to an array of axially chiral aryl-C3-benzoindoles in excellent yields with excellent enantioselectivities. The success of this strategy derives from the stepwise process involving CPA-catalyzed asymmetric formal [3 + 2] cycloaddition and subsequent central-to-axial chirality conversion by elimination of a carbamate. In addition, the practicality of this reaction had been verified by varieties of transformations towards functionalized atropisomers." @default.
- W3209515934 created "2021-11-08" @default.
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- W3209515934 creator A5062163899 @default.
- W3209515934 date "2021-01-01" @default.
- W3209515934 modified "2023-10-04" @default.
- W3209515934 title "Organocatalytic cycloaddition–elimination cascade for atroposelective construction of heterobiaryls" @default.
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