Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja307210n
DC FieldValue
dc.titleEfficient medium ring size bromolactonization using a sulfur-based zwitterionic organocatalyst
dc.contributor.authorCheng, Y.A.
dc.contributor.authorChen, T.
dc.contributor.authorTan, C.K.
dc.contributor.authorHeng, J.J.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-10-16T08:27:04Z
dc.date.available2014-10-16T08:27:04Z
dc.date.issued2012-10-10
dc.identifier.citationCheng, Y.A., Chen, T., Tan, C.K., Heng, J.J., Yeung, Y.-Y. (2012-10-10). Efficient medium ring size bromolactonization using a sulfur-based zwitterionic organocatalyst. Journal of the American Chemical Society 134 (40) : 16492-16495. ScholarBank@NUS Repository. https://doi.org/10.1021/ja307210n
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93676
dc.description.abstractCatalytic bromolactonization of long-chain olefinic acids resulting in the efficient synthesis of medium-sized lactones is reported using a zwitterionic catalyst and stoichiometric N-bromosuccinimide halogen source. The reaction was found to be more efficient at 0 °C than at room temperature, which could be attributed to the temperature dependence of the zwitterionic catalyst. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja307210n
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja307210n
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume134
dc.description.issue40
dc.description.page16492-16495
dc.description.codenJACSA
dc.identifier.isiut000309566400012
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