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https://doi.org/10.1021/acs.joc.5b00264
| Title: | Direct allylation of quinones with allylboronates | Authors: | Deng, H.-P Wang, D Szabó, K.J |
Keywords: | Ketones Allylboronates Benzoquinones Naphthoquinone Substituted carbons Allylation allylboronate derivative benzoquinone boronic acid derivative naphthoquinone quinone derivative unclassified drug allyl compound boronic acid derivative quinone derivative allylation Article chemical reaction chemical structure reaction analysis chemistry synthesis Allyl Compounds Boronic Acids Molecular Structure Quinones |
Issue Date: | 2015 | Publisher: | American Chemical Society | Citation: | Deng, H.-P, Wang, D, Szabó, K.J (2015). Direct allylation of quinones with allylboronates. Journal of Organic Chemistry 80 (6) : 3343-3348. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.joc.5b00264 | Rights: | Attribution 4.0 International | Abstract: | Allylboronates undergo C-H allylation of unsubstituted or monosubstituted benzoquinone and naphthoquinone substrates. In the case of 2,5-or 2,6-disubstituted quinones addition involving the substituted carbon takes place. Allylation with stereodefined allylboronates occurs with retention of the configuration. © 2015 American Chemical Society. | Source Title: | Journal of Organic Chemistry | URI: | https://scholarbank.nus.edu.sg/handle/10635/183885 | ISSN: | 0022-3263 | DOI: | 10.1021/acs.joc.5b00264 | Rights: | Attribution 4.0 International |
| Appears in Collections: | Staff Publications Elements |
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