Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2012.06.131
Title: Oxidative transformation of azides to aryl nitriles using DIB/TBHP: Scope and mechanistic insights
Authors: Zhao, Y.
Chew, X.
Leung, G.Y.C.
Yeung, Y.-Y. 
Keywords: Hypervalent iodine
Mechanism
Nitrile
Oxidation
Selectivity
Issue Date: 29-Aug-2012
Source: Zhao, Y., Chew, X., Leung, G.Y.C., Yeung, Y.-Y. (2012-08-29). Oxidative transformation of azides to aryl nitriles using DIB/TBHP: Scope and mechanistic insights. Tetrahedron Letters 53 (35) : 4766-4769. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2012.06.131
Abstract: Bis(tert-butylperoxy)iodobenzene, generated in situ by the reaction between diacetoxyl iodobenzene (DIB) and tert-butyl hydroperoxide (TBHP), was used in the oxidative transformation of primary azides to nitriles, and secondary azides to ketones. © 2012 Elsevier B.V. All rights reserved.
Source Title: Tetrahedron Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/76715
ISSN: 00404039
DOI: 10.1016/j.tetlet.2012.06.131
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