Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol0611494
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dc.title[3+2] Cycloaddition reactions in the solid-phase synthesis of 1,2,3-triazoles
dc.contributor.authorGao, Y.
dc.contributor.authorLam, Y.
dc.date.accessioned2014-06-23T05:29:43Z
dc.date.available2014-06-23T05:29:43Z
dc.date.issued2006-07-20
dc.identifier.citationGao, Y., Lam, Y. (2006-07-20). [3+2] Cycloaddition reactions in the solid-phase synthesis of 1,2,3-triazoles. Organic Letters 8 (15) : 3283-3285. ScholarBank@NUS Repository. https://doi.org/10.1021/ol0611494
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75387
dc.description.abstractAn efficient and regioselective procedure for the synthesis of 1,2,3-triazoles via a [3+2] cycloaddition of polymer-bound vinyl sulfone and sodium azide is described. Microwave irradiation provided significant rate enhancement in all steps of the three-step protocol. A representative set of 23 compounds was prepared. © 2006 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol0611494
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol0611494
dc.description.sourcetitleOrganic Letters
dc.description.volume8
dc.description.issue15
dc.description.page3283-3285
dc.identifier.isiut000239001500032
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