Published May 14, 2020
| Published + Supplemental Material
Journal Article
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Catalytic enantioselective synthesis of tetrasubstituted chromanones via palladium-catalyzed asymmetric conjugate arylation using chiral pyridine-dihydroisoquinoline ligands
Abstract
Highly enantioselective conjugate addition reactions of arylboronic acids to 2-substituted chromones catalyzed by palladium complexes with new chiral Pyridine-Dihydroisoquinoline (PyDHIQ) ligands have been developed. These reactions provide highly enantioselective access to chromanones containing tetrasubstituted stereocenters. Various arylboronic acids and 2-substituted chromones can be used in the catalytic reaction to afford the chiral tetrasubstituted chromanones in good yields and excellent enantioselectivities (25 examples, up to 98% yields, up to 99% ee).
Additional Information
© 2020 The Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Submitted 22 Jan 2020; Accepted 07 Apr 2020; First published 07 Apr 2020. This research was supported by the "GIST-Caltech Research Collaboration" grant funded by the GIST in 2017. This research was also supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (Ministry of Science and ICT) (NRF-2020R1A2C1009123). The NIH-NIGMS (R01GM080269) and Caltech are also thanked for support of our research program. There are no conflicts to declare.Attached Files
Published - d0sc00412j.pdf
Supplemental Material - d0sc00412j1_si.pdf
Supplemental Material - d0sc00412j2.cif
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d0sc00412j1_si.pdf
Additional details
- PMCID
- PMC7574023
- Eprint ID
- 102658
- Resolver ID
- CaltechAUTHORS:20200420-124420412
- Gwangju Institute of Science and Technology
- Caltech
- NRF-2020R1A2C1009123
- National Research Foundation of Korea
- R01GM080269
- NIH
- Created
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2020-04-20Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field