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dc.contributor.authorWu, Na (Anna)
dc.contributor.authorLi, R.
dc.contributor.authorCui, F.
dc.contributor.authorPan, Y.
dc.date.accessioned2020-05-26T10:52:33Z
dc.date.accessioned2020-06-12T09:13:22Z
dc.date.available2020-05-26T10:52:33Z
dc.date.available2020-06-12T09:13:22Z
dc.date.issued2017-07
dc.identifier.citationWu N, Li R, Cui F et al (2017) Application of dehydroabietic acid in palladium-catalysed enyne cycloisomerisation. Advanced Synthesis & Catalysis. 359(14): 2442-2447.en_US
dc.identifier.urihttp://hdl.handle.net/10454/17845
dc.descriptionYesen_US
dc.description.abstractDehydroabietic acid (DAA) promotes palladium(0)‐catalysed cyclisations of arene‐tethered 1,7‐enynols and 1,m‐enynoates (m=6,7) to give fused carbocyclic dienes. 6,6,6,5‐Tetracyclic lactones are accessible by one‐pot cycloisomerisation/Diels–Alder reaction/lactonisation from 1,7‐enynols. Furthermore, asymmetric counteranion‐directed catalysis has been developed, which afforded an indene derivative with an all‐carbon quaternary stereogenic center.en_US
dc.description.sponsorshipNSFC. Grant Number: 21462004 State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources. Grant Number: CMEMR2014A04 2015 GXNSFBA. Grant Number: 139032 GXNUen_US
dc.language.isoenen_US
dc.rights© 2017 Wiley This is the peer reviewed version of the following article: Wu N, Li R, Cui F et al (2017) Application of dehydroabietic acid in palladium-catalysed enyne cycloisomerisation. Advanced Synthesis & Catalysis. 359(14): 2442-2447, which has been published in final form at https://doi.org/10.1002/adsc.201700061. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
dc.subjectAsymmetric counteranion-directed catalysisen_US
dc.subjectCycloisomerisationen_US
dc.subjectDehydroabietic aciden_US
dc.subjectDiels-Alder reactionen_US
dc.subjectEnynolsen_US
dc.subjectLactonisationen_US
dc.subjectPalladiumen_US
dc.titleApplication of dehydroabietic acid in palladium-catalysed enyne cycloisomerisationen_US
dc.status.refereedYesen_US
dc.date.Accepted2017
dc.date.application2017-04-05
dc.typeArticleen_US
dc.type.versionAccepted Manuscripten_US
dc.identifier.doihttps://doi.org/10.1002/adsc.201700061
dc.date.updated2020-05-26T09:52:34Z
refterms.dateFOA2020-06-15T10:38:26Z


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