Total Synthesis and Structure Revision of Halioxepine

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dc.identifier.uri http://dx.doi.org/10.15488/10637
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/10715
dc.contributor.author Poock, Caroline
dc.contributor.author Kalesse, Markus
dc.date.accessioned 2021-03-26T08:44:48Z
dc.date.available 2021-03-26T08:44:48Z
dc.date.issued 2020
dc.identifier.citation Poock, C.; Kalesse, M.: Total Synthesis and Structure Revision of Halioxepine. In: Chemistry - A European Journal 27 (2020), Nr. 5, S. 1615-1619. DOI: https://doi.org/10.1002/chem.202004847
dc.description.abstract The first total synthesis of halioxepine is accomplished using a 1,4-addition for constructing the quaternary center at C10 and a halo etherification for the generation of the tertiary ether at C7. The correct structure of halioxepine was determined by assembling different enantiomeric building blocks and by changing the relative configuration between C10 and C15. © 2020 The Authors. Published by Wiley-VCH GmbH eng
dc.language.iso eng
dc.publisher Weinheim : Wiley-VCH Verl.
dc.relation.ispartofseries Chemistry - A European Journal 27 (2020), Nr. 5
dc.rights CC BY-NC-ND 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject halo etherification eng
dc.subject natural product synthesis eng
dc.subject quaternary stereocenter eng
dc.subject structure elucidation eng
dc.subject terpenoids eng
dc.subject.ddc 540 | Chemie ger
dc.title Total Synthesis and Structure Revision of Halioxepine
dc.type article
dc.type Text
dc.relation.essn 1521-3765
dc.relation.issn 0947-6539
dc.relation.doi https://doi.org/10.1002/chem.202004847
dc.bibliographicCitation.issue 5
dc.bibliographicCitation.volume 27
dc.bibliographicCitation.firstPage 1615
dc.bibliographicCitation.lastPage 1619
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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