Towards the total synthesis of Calyculin C: preparation of the C-13-C-25 spirocyclic core

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dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorHabrant, Damienen_US
dc.contributor.authorStewart, Alan J.W.en_US
dc.contributor.authorKoskinen, Ari M.P.en_US
dc.contributor.departmentDepartment of Chemistryen
dc.date.accessioned2016-09-23T09:24:23Z
dc.date.issued2009en_US
dc.description.abstractA stereoselective synthesis of the C13–C25 of Calyculin C is described. Key steps involve the coupling of a terminal acetylene with a thiol ester and subsequent spirocyclisation using a double intramolecular hetero-Michael addition.en
dc.description.versionPeer revieweden
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationHabrant, D, Stewart, A J W & Koskinen, A M P 2009, ' Towards the total synthesis of Calyculin C: preparation of the C-13-C-25 spirocyclic core ', Tetrahedron, vol. 65, no. 38, pp. 7927-7934 . https://doi.org/10.1016/j.tet.2009.07.070en
dc.identifier.doi10.1016/j.tet.2009.07.070en_US
dc.identifier.issn0040-4020
dc.identifier.otherPURE UUID: 64cd1a72-453b-41ef-b190-cd1557a12f69en_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/64cd1a72-453b-41ef-b190-cd1557a12f69en_US
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/7171051/ms144.pdfen_US
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/22424
dc.identifier.urnURN:NBN:fi:aalto-201609234427
dc.language.isoenen
dc.publisherElsevier
dc.relation.ispartofseriesTetrahedronen
dc.relation.ispartofseriesVolume 65, issue 38, pp. 7927-7934en
dc.rightsopenAccessen
dc.titleTowards the total synthesis of Calyculin C: preparation of the C-13-C-25 spirocyclic coreen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
dc.type.versionacceptedVersion

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[article-cris] Kemian tekniikan korkeakoulu / CHEM