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An improved synthesis of diiodonoradamantane

dc.contributor.authorIoannou, Savvasen
dc.contributor.authorNicolaides, Athanassios V.en
dc.creatorIoannou, Savvasen
dc.creatorNicolaides, Athanassios V.en
dc.date.accessioned2019-11-21T06:19:29Z
dc.date.available2019-11-21T06:19:29Z
dc.date.issued2009
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55580
dc.description.abstractΤhe synthesis of 3,7-diiodo-tricyclo[3.3.1.03,7]nonane, the main precursor of noradamantene, by iodination of the corresponding diol via its dimesylate affords a threefold higher yield than the direct iodination of the diol. Neither the dimesylate nor the cyclic sulfate of the diol yields noradamantene upon reduction with sodium amalgam. © 2009 Elsevier Ltd. All rights reserved.en
dc.sourceTetrahedron lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-70350512005&doi=10.1016%2fj.tetlet.2009.08.108&partnerID=40&md5=2e78e9fd5d85ec996ad1f2181fcf85d5
dc.subjectarticleen
dc.subjectunclassified drugen
dc.subjectsynthesisen
dc.subjectchemical structureen
dc.subjectchemical modificationen
dc.subjectiodinationen
dc.subjectdiiodonoradamantaneen
dc.subjectnonaneen
dc.titleAn improved synthesis of diiodonoradamantaneen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.tetlet.2009.08.108
dc.description.volume50
dc.description.issue50
dc.description.startingpage6938
dc.description.endingpage6940
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :9</p>en
dc.source.abbreviationTetrahedron Lett.en
dc.contributor.orcidNicolaides, Athanassios V. [0000-0003-0841-565X]
dc.gnosis.orcid0000-0003-0841-565X


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