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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3gc41126e
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dc.titleOrganocatalytic 1,3-dipolar cycloaddition reactions of ketones and azides with water as a solvent
dc.contributor.authorYeung, D.K.J.
dc.contributor.authorGao, T.
dc.contributor.authorHuang, J.
dc.contributor.authorSun, S.
dc.contributor.authorGuo, H.
dc.contributor.authorWang, J.
dc.date.accessioned2014-10-16T08:36:07Z
dc.date.available2014-10-16T08:36:07Z
dc.date.issued2013-09
dc.identifier.citationYeung, D.K.J., Gao, T., Huang, J., Sun, S., Guo, H., Wang, J. (2013-09). Organocatalytic 1,3-dipolar cycloaddition reactions of ketones and azides with water as a solvent. Green Chemistry 15 (9) : 2384-2388. ScholarBank@NUS Repository. https://doi.org/10.1039/c3gc41126e
dc.identifier.issn14639262
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94444
dc.description.abstractWe reported an enamine catalyzed strategy to fully promote a 1,3-dipolar cycloaddition to access a vast pool of substituted 1,2,3-triazoles with water as the only solvent. © 2013 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3gc41126e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c3gc41126e
dc.description.sourcetitleGreen Chemistry
dc.description.volume15
dc.description.issue9
dc.description.page2384-2388
dc.description.codenGRCHF
dc.identifier.isiut000323179000011
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