Journal
CHEMICAL SCIENCE
Volume 5, Issue 1, Pages 112-116Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3sc52265b
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Funding
- NIH-NIGMS [PO1 GM69721, R01-GM43214, R01-GM096129]
- Spanish Ministry of Education and Science (MEC) [AP2009-0950]
- Alexander von Humboldt Foundation
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The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through the merger of photoredox and asymmetric anion-binding catalysis. This combination of two distinct catalysis concepts introduces a potentially general approach to asymmetric transformations in oxidative photocatalysis.
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