Journal article
Enantioselective one-pot synthesis of dihydroquinolones via BINOL-derived Lewis acid catalysis
- Abstract:
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A high-yielding and diastereoselective route to biologically significant 2-aryl- and 2-alkyl-3-amido dihydroquinolones has been developed in up to 90 : 10 e.r. by employing a novel Lewis acidic BINOL-derived copper(II) catalyst.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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Access Document
- Files:
-
-
(Preview, Accepted manuscript, pdf, 789.2KB, Terms of use)
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- Publisher copy:
- 10.1039/c4ob00627e
Authors
Bibliographic Details
- Publisher:
- Royal Society of Chemistry
- Journal:
- Organic and Biomolecular Chemistry More from this journal
- Volume:
- 12
- Issue:
- 28
- Pages:
- 5094-5097
- Publication date:
- 2014-06-13
- Acceptance date:
- 2014-06-03
- DOI:
- EISSN:
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1477-0539
- ISSN:
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1477-0520
- Pmid:
-
24927823
Item Description
- Language:
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English
- Keywords:
- Pubs id:
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pubs:469511
- UUID:
-
uuid:d2764cf3-0736-4654-8d49-185dbbcf5da6
- Local pid:
-
pubs:469511
- Source identifiers:
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469511
- Deposit date:
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2018-03-27
Terms of use
- Copyright holder:
- Royal Society of Chemistry
- Copyright date:
- 2014
- Notes:
- © The Royal Society of Chemistry 2014. This is the accepted manuscript version of the article. The final version is available online from Royal Society of Chemistry at: https://doi.org/10.1039/c4ob00627e
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