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Quinone-catalyzed oxidative deformylation: synthesis of imines from amino alcohols

dc.contributor.authorLiu, Xinyun
dc.contributor.authorPhan, Johnny H.
dc.contributor.authorHaugeberg, Benjamin John
dc.contributor.authorLondhe, Shrikant S.
dc.contributor.authorClift, Michael D.
dc.date.accessioned2018-06-13T19:10:19Z
dc.date.available2018-06-13T19:10:19Z
dc.date.issued2017-12-28
dc.identifier.citationLiu, X., Phan, J. H., Haugeberg, B. J., Londhe, S. S., & Clift, M. D. (2017). Quinone-catalyzed oxidative deformylation: synthesis of imines from amino alcohols. Beilstein Journal of Organic Chemistry, 13, 2895–2901. http://doi.org/10.3762/bjoc.13.282en_US
dc.identifier.urihttp://hdl.handle.net/1808/26511
dc.description.abstractA new method for imine synthesis by way of quinone-catalyzed oxidative deformylation of 1,2-amino alcohols is reported. A wide range of readily accessible amino alcohols and primary amines can be reacted to provide N-protected imine products. The methodology presented provides a novel organocatalytic approach for imine synthesis and demonstrates the synthetic versatility of quinone-catalyzed oxidative C–C bond cleavage.en_US
dc.publisherBeilstein-Instituten_US
dc.rightsCopyright © 2017, Liu et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0en_US
dc.subjectCatalysisen_US
dc.subjectDeformylationen_US
dc.subjectOrganic synthesisen_US
dc.subjectOrganocatalysisen_US
dc.titleQuinone-catalyzed oxidative deformylation: synthesis of imines from amino alcoholsen_US
dc.typeArticleen_US
kusw.kuauthorLiu, Xinyun
kusw.kuauthorPhan, Johnny H.
kusw.kuauthorHaugeberg, Benjamin J.
kusw.kuauthorLondhe, Shrikant S.
kusw.kuauthorClift, Michael D.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3762/bjoc.13.282en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccessen_US


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Copyright © 2017, Liu et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)
Except where otherwise noted, this item's license is described as: Copyright © 2017, Liu et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)