Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/148229
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dc.contributor.authorCao, Liyaen_US
dc.contributor.authorLi, Tingtingen_US
dc.contributor.authorChi, Robin Yongguien_US
dc.contributor.authorJin, Zhichaoen_US
dc.date.accessioned2021-06-04T07:07:54Z-
dc.date.available2021-06-04T07:07:54Z-
dc.date.issued2021-
dc.identifier.citationCao, L., Li, T., Chi, R. Y. & Jin, Z. (2021). Carbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivatives. Asian Journal of Organic Chemistry, 10(5), 1090-1093. https://dx.doi.org/10.1002/ajoc.202100113en_US
dc.identifier.issn2193-5815en_US
dc.identifier.other0000-0003-3003-6437-
dc.identifier.urihttps://hdl.handle.net/10356/148229-
dc.description.abstractAn N-heterocyclic carbene-catalyzed [3+3] cycloaddition reaction of acylthioureas with ynals is reported. Both N atoms in the thiourea substrate are activated as nucleophiles and incorporated inside the ring system of the product. Pyrimidinthione derivatives bearing various substituents and substitution patterns are afforded as the products in moderate to good yields.en_US
dc.description.sponsorshipMinistry of Education (MOE)en_US
dc.description.sponsorshipNational Research Foundation (NRF)en_US
dc.language.isoenen_US
dc.relation.ispartofAsian Journal of Organic Chemistryen_US
dc.rightsThis is the peer reviewed version of the following article: Cao, L., Li, T., Chi, R. Y. & Jin, Z. (2021). Carbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivatives. Asian Journal of Organic Chemistry, 10(5), 1090-1093. https://dx.doi.org/10.1002/ajoc.202100113, which has been published in final form at https://doi.org/10.1002/ajoc.202100113. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en_US
dc.subjectScience::Chemistryen_US
dc.titleCarbene-catalyzed N,N-nucleophilic activation of thioureas for access to pyrimidinthione derivativesen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1002/ajoc.202100113-
dc.description.versionAccepted versionen_US
dc.identifier.scopus2-s2.0-85103543728-
dc.identifier.issue5en_US
dc.identifier.volume10en_US
dc.identifier.spage1090en_US
dc.identifier.epage1093en_US
dc.subject.keywordsNucleophilic Additionen_US
dc.subject.keywordsOrganocatalysisen_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
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