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Chiral arylsulfinylamides as reagents for visible light-mediated asymmetric alkene aminoarylations - Nature Chemistry

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Chiral arylsulfinylamides as reagents for visible light-mediated asymmetric alkene aminoarylations - Nature Chemistry

Two- or one-electron-mediated difunctionalizations of internal alkenes represent straightforward approaches to assemble molecular complexity by the simultaneous formation of two contiguous Csp3 stereocentres. Although racemic versions have been extensively explored, asymmetric variants, especially those involving

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Chiral arylsulfinylamides as reagents for visible light-mediated asymmetric alkene aminoarylations - Nature Chemistry

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Chiral arylsulfinylamides as reagents for visible light-mediated asymmetric alkene aminoarylations - Nature Chemistry

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