dc.contributor.authorXiang, Shaohua
dc.contributor.authorHe, Jingxi
dc.contributor.authorMa, Jimei
dc.contributor.authorLiu, Xue-Wei
dc.date.accessioned2014-12-09T01:52:44Z
dc.date.available2014-12-09T01:52:44Z
dc.date.copyright2014en_US
dc.date.issued2014
dc.identifier.citationXiang, S., He, J., Ma, J., & Liu, X.-W. (2014). One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation. Chemical communications, 50(32), 4222-4224.en_US
dc.identifier.urihttp://hdl.handle.net/10220/24357
dc.description.abstractA concise and highly efficient strategy for the synthesis of N-glycosyl imidazole analogues is reported. This reaction is based on a palladium catalysed decarboxylative allylation and three steps, namely, carbamation, decarboxylation and allylation are involved. All the substrates can afford the desired products with excellent yields and selectivities.en_US
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en_US
dc.description.sponsorshipMOH (Min. of Health, S’pore)en_US
dc.format.extent3 p.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesChemical communicationsen_US
dc.rights© 2014 The Authors. This is the author created version of a work that has been peer reviewed and accepted for publication in Chemical Communications, published by Royal Society of Chemistry on behalf of The Authors. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1039/c3cc48041k].en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
dc.titleOne-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylationen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1039/c3cc48041k
dc.description.versionAccepted versionen_US


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