Ali, Wajid ; Behera, Ahalya ; Guin, Srimanta ; Patel, Bhisma K. (2015) Regiospecific benzoylation of electron-deficient N-heterocycles with methylbenzenes via a minisci-type reaction The Journal of Organic Chemistry, 80 (11). pp. 5625-5632. ISSN 0022-3263
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Official URL: https://pubs.acs.org/doi/abs/10.1021/acs.joc.5b005...
Related URL: http://dx.doi.org/10.1021/acs.joc.5b00501
Abstract
A regioselective cross-dehydrogenative coupling between electron-deficient N-heterocycles (isoquinoline, quinolines, and quinoxalines) and methylbenzenes leading to regiospecific C–aroylation has been accomplished using AlCl3 as the catalyst in the presence of oxidant TBHP. This protocol is a practical alternative to the classical Minisci reaction.
Item Type: | Article |
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Source: | Copyright of this article belongs to American Chemical Society. |
ID Code: | 114037 |
Deposited On: | 02 May 2018 04:52 |
Last Modified: | 02 May 2018 04:52 |
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