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Journal article

Enantioselective one-pot synthesis of dihydroquinolones via BINOL-derived Lewis acid catalysis.

Abstract:
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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Publisher copy:
10.1039/c4ob00627e

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author
Publisher:
Royal Society of Chemistry Publisher's website
Journal:
Organic and Biomolecular Chemistry Journal website
Volume:
12
Issue:
28
Pages:
5094-5097
Publication date:
2014-06-13
DOI:
EISSN:
1477-0539
ISSN:
1477-0520
Source identifiers:
469511
Language:
English
Keywords:
Pubs id:
pubs:469511
UUID:
uuid:cf5811e0-7d49-4bf8-9c9a-3a76fe7fafcd
Local pid:
pubs:469511
Deposit date:
2014-06-30

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