4.6 Article

Enantioselective [2+2] photocycloaddition of quinolone using a C1-symmetric chiral phosphoric acid as a visible-light photocatalyst

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 20, Issue 19, Pages 3940-3947

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ob00607c

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In this study, an enantioselective intra- and intermolecular [2 + 2] photocycloaddition of quinolone using a C-1-symmetric chiral phosphoric acid as a visible-light photocatalyst was developed. The thioxanthone chromophore on the phosphoric acid played a crucial role in both phototransformation and enantioselectivity.
The enantioselective intra- and intermolecular [2 + 2] photocycloaddition of quinolone using a C-1-symmetric chiral phosphoric acid as a visible-light photocatalyst is developed. The thioxanthone chromophore on phosphoric acid plays an important role in both phototransformation and enantioselectivity.

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