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Reference: Knipe, PC and Smith, MD, (2014). Enantioselective one-pot synthesis of dihydroquinolones via BINOL-derived Lewis acid catalysis. Organic and Biomolecular Chemistry, 12 (28), 5094-5097.Citable link to this page:

 

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.

Peer Review status:Peer reviewedPublication status:PublishedVersion:Accepted manuscript Funder: European Research Council   Notes:This journal is © The Royal Society of Chemistry, 2014. This is the accepted manuscript version of the article. The final version is available online from the Royal Society of Chemistry at: [10.1039/C4OB00627E].

Bibliographic Details

Publisher: Royal Society of Chemistry

Publisher Website: http://www.rsc.org/

Journal: Organic and Biomolecular Chemistrysee more from them

Publication Website: http://pubs.rsc.org/en/Journals/JournalIssues/OB

Issue Date: 2014-06-13

pages:5094-5097Identifiers

Urn: uuid:cf5811e0-7d49-4bf8-9c9a-3a76fe7fafcd

Source identifier: 469511

Eissn: 1477-0539

Doi: https://doi.org/10.1039/c4ob00627e

Issn: 1477-0520 Item Description

Type: Journal article;

Language: eng

Version: Accepted manuscriptKeywords: Copper Aldehydes Aniline Compounds Quinolones Naphthols Molecular Structure Cyclization Catalysis Stereoisomerism Electrochemical Techniques Lewis Acids Tiny URL: pubs:469511

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Autor: Knipe, PC - institutionUniversity of Oxford Oxford, MPLS, Chemistry, Organic Chemistry - - - Smith, MD - institutionUniversity of

Fuente: https://ora.ox.ac.uk/objects/uuid:cf5811e0-7d49-4bf8-9c9a-3a76fe7fafcd



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