Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 72, Pages 7953-7955Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc43996h
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Funding
- Taiwan Ministry of Education
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A new asymmetric photocyclization-reduction cascade employing readily available aminochalcones has been developed. The reaction sequence has been achieved by unifying photochemistry and asymmetric Bronsted acid catalysis and involves photocyclization followed by Bronsted acid catalyzed enantioselective hydrogenation in batch and flow.
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