A New Approach to the Synthesis of Benzo[b]naphtho[2,3-b]furan-6,11-diones and 2-Benzyl-3-hydroxynaphthalene-1,4-diones
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Centro de Investigación en Química Biolóxica e Materiais Moleculares | gl |
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Química Orgánica | gl |
| dc.contributor.author | Barcia Barcia, José Carlos | |
| dc.contributor.author | Cruces, Jacobo | |
| dc.contributor.author | Salas, Cristian O. | |
| dc.contributor.author | Estévez Cabanas, Juan Carlos | |
| dc.contributor.author | Cuéllar, Mauricio A. | |
| dc.contributor.author | Tapia, Ricardo A. | |
| dc.contributor.author | Estévez Cabanas, Ramón José | |
| dc.date.accessioned | 2020-05-24T19:56:10Z | |
| dc.date.available | 2020-05-24T19:56:10Z | |
| dc.date.issued | 2017 | |
| dc.description.abstract | Here we describe modified syntheses of o-acetylbenzoic acids and o-acetylphenylacetic acids by Heck palladium-catalysed arylation of n-butyl vinyl ether with o-iodobenzoic acids or with o-iodophenylacetic acids, respectively. General syntheses of benzo[b]naphtho[2,3-b]furan-6,11-diones from o-acetylbenzoic acids and 2-benzyl3-hydroxynaphthalene-1,4-diones from o-acetylphenylacetic acids are also reported. | gl |
| dc.description.peerreviewed | SI | gl |
| dc.description.sponsorship | This work has received financial support from the Xunta de Galicia (Centro singular de investigación de Galicia accreditation 2016–2019, ED431G/09; and Project GRC2014/040), the European Union (Europe- an Regional Development Fund-ERDF), FONDECYT (Research Grants 1161816 and 1141264) and Galchimia S.A. | gl |
| dc.identifier.citation | Barcia, J., Cruces, J., Salas, C., Estévez, J., Cuellar, M., Tapia, R., & Estévez, R. (2017). A New Approach to the Synthesis of Benzo[b]naphtho[2,3-b]furan-6,11-diones and 2-Benzyl-3-hydroxynaphthalene-1,4-diones. Synopen, 01(01), 0156-0165. https://doi.org/10.1055/s-0036-1591729 | gl |
| dc.identifier.doi | 10.1055/s-0036-1591729 | |
| dc.identifier.issn | 2509-9396 | |
| dc.identifier.uri | http://hdl.handle.net/10347/22517 | |
| dc.language.iso | eng | gl |
| dc.publisher | Georg Thieme Verlag | gl |
| dc.relation.publisherversion | https://doi.org/10.1055/s-0036-1591729 | gl |
| dc.rights | © 2017 by the authors. This is an open access article distributed under the terms and conditions of the Creative Commons CC BY-ND-NC 4.0 license (Attribution-NonCommercial-NoDerivatives) | gl |
| dc.rights.accessRights | open access | gl |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.subject | Fused-ring systems | gl |
| dc.subject | Heck reaction | gl |
| dc.subject | Quinones | gl |
| dc.subject | Palladium | gl |
| dc.subject | Heterocycles | gl |
| dc.subject | Halides | gl |
| dc.subject | Furans | gl |
| dc.title | A New Approach to the Synthesis of Benzo[b]naphtho[2,3-b]furan-6,11-diones and 2-Benzyl-3-hydroxynaphthalene-1,4-diones | gl |
| dc.type | journal article | gl |
| dc.type.hasVersion | VoR | gl |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 86b5b898-6642-4dd7-b2ee-117e2f4838ff | |
| relation.isAuthorOfPublication | 19cdf079-dc1b-48b2-8bc9-c73d3601f141 | |
| relation.isAuthorOfPublication.latestForDiscovery | 86b5b898-6642-4dd7-b2ee-117e2f4838ff |
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