Please use this identifier to cite or link to this item: 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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