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https://doi.org/10.1021/ja307210n
DC Field | Value | |
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dc.title | Efficient medium ring size bromolactonization using a sulfur-based zwitterionic organocatalyst | |
dc.contributor.author | Cheng, Y.A. | |
dc.contributor.author | Chen, T. | |
dc.contributor.author | Tan, C.K. | |
dc.contributor.author | Heng, J.J. | |
dc.contributor.author | Yeung, Y.-Y. | |
dc.date.accessioned | 2014-10-16T08:27:04Z | |
dc.date.available | 2014-10-16T08:27:04Z | |
dc.date.issued | 2012-10-10 | |
dc.identifier.citation | Cheng, 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.issn | 00027863 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/93676 | |
dc.description.abstract | Catalytic 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja307210n | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ja307210n | |
dc.description.sourcetitle | Journal of the American Chemical Society | |
dc.description.volume | 134 | |
dc.description.issue | 40 | |
dc.description.page | 16492-16495 | |
dc.description.coden | JACSA | |
dc.identifier.isiut | 000309566400012 | |
Appears in Collections: | Staff Publications |
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