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https://doi.org/10.1021/ol200840e
| Title: | Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids | Authors: | Tan, C.K. Zhou, L. Yeung, Y.-Y. |
Issue Date: | 20-May-2011 | Citation: | Tan, C.K., Zhou, L., Yeung, Y.-Y. (2011-05-20). Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids. Organic Letters 13 (10) : 2738-2741. ScholarBank@NUS Repository. https://doi.org/10.1021/ol200840e | Abstract: | An efficient and enantioselective bromolactonization of 1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst has been developed, resulting in the formation of δ-lactones containing two chiral centers with up to 99% yield, 95% ee. © 2011 American Chemical Society. | Source Title: | Organic Letters | URI: | http://scholarbank.nus.edu.sg/handle/10635/93077 | ISSN: | 15237060 | DOI: | 10.1021/ol200840e |
| Appears in Collections: | Staff Publications |
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