Highly enantioselective access to chiral chromanes and thiochromanes via Cu-catalyzed hydroamination with anthranils
Author:
Affiliation:
1. Department of Chemistry
2. Southern University of Science and Technology
3. Shenzhen 518055
4. China
5. Hong Kong Baptist University
6. Kowloon
7. Hong Kong
8. Institute of Research and Continuing Education
Abstract
Highly efficient and atom-economic asymmetric access to 4-arylamino chromanes and thiochromanes bearing a benzylic alcohol functionality were developed by Cu(i)/(R,R)-Ph-BPE-catalyzed enantioselective hydroamination with anthranils.
Funder
Hong Kong Baptist University
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00030F
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