Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0cc03691a
DC FieldValue
dc.titleMechanistic considerations of guanidine-catalyzed reactions
dc.contributor.authorFu, X.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:57:19Z
dc.date.available2014-06-23T05:57:19Z
dc.date.issued2011-08-07
dc.identifier.citationFu, X., Tan, C.-H. (2011-08-07). Mechanistic considerations of guanidine-catalyzed reactions. Chemical Communications 47 (29) : 8210-8222. ScholarBank@NUS Repository. https://doi.org/10.1039/c0cc03691a
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77616
dc.description.abstractThis feature article discusses the various mechanistic aspects of guanidine-catalyzed reactions. Guanidines are well known as strong organic bases; however, in the first section, three most common commercially available guanidines, TMG, TBD and MTBD, will be used to illustrate the use of guanidines as nucleophilic catalysts. In the second section, different modes of hydrogen bonding interactions of the conjugate acid of guanidine, the guanidinium, are discussed. Particularly interesting are the possibilities of mono-functional or bifunctional activation of a nucleophile and an electrophile by guanidinium. © 2011 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0cc03691a
dc.sourceScopus
dc.typeReview
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c0cc03691a
dc.description.sourcetitleChemical Communications
dc.description.volume47
dc.description.issue29
dc.description.page8210-8222
dc.description.codenCHCOF
dc.identifier.isiut000292980900002
Appears in Collections:Staff Publications

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