Application of dehydroabietic acid in palladium-catalysed enyne cycloisomerisation
dc.contributor.author | Wu, Na (Anna) | |
dc.contributor.author | Li, R. | |
dc.contributor.author | Cui, F. | |
dc.contributor.author | Pan, Y. | |
dc.date.accessioned | 2020-05-26T10:52:33Z | |
dc.date.accessioned | 2020-06-12T09:13:22Z | |
dc.date.available | 2020-05-26T10:52:33Z | |
dc.date.available | 2020-06-12T09:13:22Z | |
dc.date.issued | 2017-07 | |
dc.identifier.citation | 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. | en_US |
dc.identifier.uri | http://hdl.handle.net/10454/17845 | |
dc.description | Yes | en_US |
dc.description.abstract | Dehydroabietic 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.sponsorship | NSFC. Grant Number: 21462004 State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources. Grant Number: CMEMR2014A04 2015 GXNSFBA. Grant Number: 139032 GXNU | en_US |
dc.language.iso | en | en_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.subject | Asymmetric counteranion-directed catalysis | en_US |
dc.subject | Cycloisomerisation | en_US |
dc.subject | Dehydroabietic acid | en_US |
dc.subject | Diels-Alder reaction | en_US |
dc.subject | Enynols | en_US |
dc.subject | Lactonisation | en_US |
dc.subject | Palladium | en_US |
dc.title | Application of dehydroabietic acid in palladium-catalysed enyne cycloisomerisation | en_US |
dc.status.refereed | Yes | en_US |
dc.date.Accepted | 2017 | |
dc.date.application | 2017-04-05 | |
dc.type | Article | en_US |
dc.type.version | Accepted Manuscript | en_US |
dc.identifier.doi | https://doi.org/10.1002/adsc.201700061 | |
dc.date.updated | 2020-05-26T09:52:34Z | |
refterms.dateFOA | 2020-06-15T10:38:26Z |