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https://doi.org/10.1016/j.tetlet.2013.01.053
| Title: | Studies on the ring-opening of bicyclic cyclopropanes activated by a carbonyl group | Authors: | Jiang, X. Lim, Z. Yeung, Y.-Y. |
Keywords: | Cyclopropane Friedel-Crafts Lewis acid Mechanism Selectivity |
Issue Date: | 3-Apr-2013 | Citation: | Jiang, X., Lim, Z., Yeung, Y.-Y. (2013-04-03). Studies on the ring-opening of bicyclic cyclopropanes activated by a carbonyl group. Tetrahedron Letters 54 (14) : 1798-1801. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2013.01.053 | Abstract: | Studies on the Friedel-Crafts reaction between carbonyl bicyclic cyclopropane and electronic-rich aromatic systems were conducted. Lewis acid and iminium cationic activation methods were examined. It was found that the cyclopropane ring-opening was highly dependent on the nature of the counter nucleophile as well as the activation method. © 2013 Elsevier Ltd. All rights reserved. | Source Title: | Tetrahedron Letters | URI: | http://scholarbank.nus.edu.sg/handle/10635/77080 | ISSN: | 00404039 | DOI: | 10.1016/j.tetlet.2013.01.053 |
| Appears in Collections: | Staff Publications |
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