Please use this identifier to cite or link to this item:
https://doi.org/10.1016/j.tetlet.2012.06.131
DC Field | Value | |
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dc.title | Oxidative transformation of azides to aryl nitriles using DIB/TBHP: Scope and mechanistic insights | |
dc.contributor.author | Zhao, Y. | |
dc.contributor.author | Chew, X. | |
dc.contributor.author | Leung, G.Y.C. | |
dc.contributor.author | Yeung, Y.-Y. | |
dc.date.accessioned | 2014-06-23T05:46:12Z | |
dc.date.available | 2014-06-23T05:46:12Z | |
dc.date.issued | 2012-08-29 | |
dc.identifier.citation | 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 | |
dc.identifier.issn | 00404039 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/76715 | |
dc.description.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. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2012.06.131 | |
dc.source | Scopus | |
dc.subject | Hypervalent iodine | |
dc.subject | Mechanism | |
dc.subject | Nitrile | |
dc.subject | Oxidation | |
dc.subject | Selectivity | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1016/j.tetlet.2012.06.131 | |
dc.description.sourcetitle | Tetrahedron Letters | |
dc.description.volume | 53 | |
dc.description.issue | 35 | |
dc.description.page | 4766-4769 | |
dc.description.coden | TELEA | |
dc.identifier.isiut | 000307601300036 | |
Appears in Collections: | Staff Publications |
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