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dc.contributor.authorSiyu, Y.
dc.contributor.authorWu, Na
dc.date.accessioned2021-03-30T19:20:41Z
dc.date.accessioned2021-04-15T11:19:48Z
dc.date.available2021-03-30T19:20:41Z
dc.date.available2021-04-15T11:19:48Z
dc.date.issued2020
dc.identifier.citationSiyu Y and Wu N (2020) The Chemistry of Ynamide and its Application in Organic Synthesis. In: Rahman AU (Ed) Advances in Organic Synthesis. Volume 13. Singapore: Bentham Science Publishers.
dc.identifier.urihttp://hdl.handle.net/10454/18435
dc.descriptionYes
dc.description.abstractYnamide, is an understudied but attractive class of alkynes, activated by the donating ability of the nitrogen adjacent to alkynes. With the nucleophilicity on β-carbon and the electrophilicity on α-carbon of ynamides, this review summarizes the syntheses of ynamides and miscellaneous reactions - oxidation, rearrangement, cyclization, and cycloaddition to construct complicated heterocyclic rings. The synthetic methodologies were further applied into natural products synthesis, e.g. marinoquinolines A and C, aplidiopsamine A, rigidin A, and 7-azaserotonin derivative.
dc.description.sponsorshipWe thank National Science Foundation of China (NSFC) (21462004), State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (CMEMR2014-A04), 2015 GXNSFBA (139032), GXNU, and Newton International Fellowship granted by Royal Society.
dc.language.isoen
dc.subjectYnamide
dc.subjectYndiamide
dc.subjectThioenamide
dc.subjectHaloenamide
dc.subjectKeteniminium
dc.subjectWitulski rearrangment
dc.subjectUllmann coupling
dc.subjectDipolar cycloaddition
dc.subjectα-ketoimide
dc.subjectPolycyclic alkaloids
dc.titleThe Chemistry of Ynamide and its Application in Organic Synthesis
dc.status.refereedYes
dc.typeBook chapter
dc.type.versionAccepted manuscript
dc.identifier.doihttps://doi.org/10.2174/9789811405082120130004
dc.rights.licenseUnspecified
dc.date.updated2021-03-30T18:20:52Z
refterms.dateFOA2021-04-15T11:20:27Z
dc.openaccess.statusopenAccess


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