Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 34, Pages 11847-11849Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja103786c
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Funding
- Ministry of Education, Science and Technology [2010-0015948]
- National Research Foundation of Korea [2009-0071779] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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The first organocatalytic enantioselective intramolecular 1,5-hydride transfer/ring closure reaction is described. This redox neutral reaction cascade allows for the efficient formation of ring-fused tetrahydroquinolines in high enantioselectivities.
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