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dc.contributor.authorLi, R.
dc.contributor.authorWen, Z.
dc.contributor.authorWu, Na (Anna)
dc.date.accessioned2020-06-02T12:56:31Z
dc.date.accessioned2020-06-22T13:24:28Z
dc.date.available2020-06-02T12:56:31Z
dc.date.available2020-06-22T13:24:28Z
dc.date.issued2016-12
dc.identifier.citationLi R, Wen Z and Wu N (2016) A nordehydroabietyl amide-containing chiral diene for rhodium-catalysed asymmetric arylation to nitroolefins. Organic and Biomolecular Chemistry. 14(47): 11080-11084.en_US
dc.identifier.urihttp://hdl.handle.net/10454/17848
dc.descriptionYesen_US
dc.description.abstractA highly enantioselective rhodium catalysed asymmetric arylation (RCAA) of nitroolefins with arylboronic acids is presented using a newly developed, C1-symmetric, non-covalent interacted, phellandrene derived, nordehydroabietyl amide-containing chiral diene under mild conditions. Stereoelectronic effects were studied, suggesting an activation of the bound substrate through the secondary amide as a hydrogen-bond donor.en_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttps://doi.org/10.1039/C6OB02202Ben_US
dc.rights(c) 2016 RSC. Full-text reproduced in accordance with the publisher's self-archiving policy.
dc.subjectNordehydroabietyl amideen_US
dc.subjectChiral dieneen_US
dc.subjectRCAAen_US
dc.subjectRhodium-catalysed asymmetric arylationen_US
dc.titleA nordehydroabietyl amide-containing chiral diene for rhodium-catalysed asymmetric arylation to nitroolefinsen_US
dc.status.refereedYesen_US
dc.date.Accepted2016-11-10
dc.date.application2016-11-14
dc.typeArticleen_US
dc.type.versionAccepted manuscripten_US
dc.date.updated2020-06-02T11:56:31Z
refterms.dateFOA2020-06-23T06:21:51Z


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