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http://hdl.handle.net/10397/101596
| Title: | Efficient selenium-catalyzed selective C(sp3)−H oxidation of benzylpyridines with molecular oxygen | Authors: | Jin, W Zheng, P Wong, WT Law, GL |
Issue Date: | 2-May-2017 | Source: | Advanced synthesis & catalysis, 2 May 2017, v. 359, no. 9, p. 1588-1593 | Abstract: | An efficient selenium-catalyzed direct oxidation of benzylpyridines in aqueous DMSO has been successfully developed by using molecular oxygen as the oxidant. A variety of benzoylpyridines with broad functional group tolerance were obtained in modest to excellent yields and with exclusive chemoselectivity. | Keywords: | C−H oxidation Heterocycles Molecular oxygen Selenium catalysis |
Publisher: | Wiley-VCH | Journal: | Advanced synthesis & catalysis | ISSN: | 1615-4150 | EISSN: | 1615-4169 | DOI: | 10.1002/adsc.201601065 | Rights: | © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim This is the peer reviewed version of the following article: W. Jin, P. Zheng, W.-T. Wong, G.-L. Law, Efficient Selenium-Catalyzed Selective C(sp3)−H Oxidation of Benzylpyridines with Molecular Oxygen. Adv. Synth. Catal. 2017, 359, 1588-1593, which has been published in final form at https://doi.org/10.1002/adsc.201601065. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited. |
| Appears in Collections: | Journal/Magazine Article |
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| Wong_Efficient_Selenium-Catalyzed_Selective.pdf | Pre-Published version | 1.46 MB | Adobe PDF | View/Open |
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