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dc.contributor.authorLi, X.
dc.contributor.authorWang, G.
dc.contributor.authorZhang, Z.
dc.contributor.authorWu, Na
dc.contributor.authorYang, Q.
dc.contributor.authorHuang, S.
dc.contributor.authorWang, X.
dc.date.accessioned2020-05-26T11:21:18Z
dc.date.accessioned2020-06-22T13:37:25Z
dc.date.available2020-05-26T11:21:18Z
dc.date.available2020-06-22T13:37:25Z
dc.date.issued2019
dc.identifier.citationLi X, Wang G, Zhang Z et al (2019) A concise and straightforward approach to total synthesis of (+)-Strictifolione and formal synthesis of Cryptofolione via a unified strategy. Synthetic Communications. 49(8): 1031-1039.
dc.identifier.urihttp://hdl.handle.net/10454/17850
dc.descriptionYes
dc.description.abstractWe describe a concise and straightforward approach to the total syntheses of (+)-Strictifolione and Cryptofolione in the longest linear sequences of four steps and six steps from 3-phenyl propanal and trans-cinnamaldehyde, respectively. The route utilized a titanium tetraisopropoxide/(R)-[1,1'-binaphthalene]-2,2'-diol catalyzed Mukaiyama aldol reaction, indium(0)-promoted Barbier reaction, and olefin cross-metathesis as the key reactions.
dc.description.sponsorshipNational Science Foundation of China [21062088, 21562020, and 21462004], the Science and Technology Plan Project of Jiangxi Province [No. 20151BBG70028, 20142BBE50006] and State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2014-A04] for the funding support.
dc.language.isoen
dc.rights© 2019 Taylor & Francis. This is an Author's Original Manuscript of an article published by Taylor & Francis in Synthetic Communications on 16 Mar 2019 available online at https://doi.org/10.1080/00397911.2019.1580373
dc.subjectStrictifolione
dc.subjectCryptofolione
dc.subjectTotal synthesis
dc.subjectBarbier reaction
dc.subjectOlefin cross-metathesis
dc.titleA concise and straightforward approach to total synthesis of (+)-Strictifolione and formal synthesis of Cryptofolione via a unified strategy
dc.status.refereedYes
dc.date.application16/03/2019
dc.typeArticle
dc.type.versionAccepted manuscript
dc.identifier.doihttps://doi.org/10.1080/00397911.2019.1580373
dc.rights.licenseUnspecified
dc.date.updated2020-05-26T10:21:18Z
refterms.dateFOA2020-06-23T08:34:07Z
dc.openaccess.statusopenAccess
dc.date.accepted04/02/2019


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