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dc.contributor.authorRiala, Mariaen
dc.contributor.authorChronakis, Nikosen
dc.creatorRiala, Mariaen
dc.creatorChronakis, Nikosen
dc.date.accessioned2019-11-21T06:22:31Z
dc.date.available2019-11-21T06:22:31Z
dc.date.issued2014
dc.identifier.issn1359-7345
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56065
dc.description.abstractWe have synthesized and isolated two C2-symmetric enantiomerically pure trisadducts of C60 with an inherently chiral trans-3,trans-3,trans-3 addition pattern with the aid of an enantiopure cyclo-tris-malonate tether. An unexpected stereoisomerism was observed which was attributed to the spatial arrangement of spacers in the tether. © 2014 The Royal Society of Chemistry.en
dc.sourceChemical Communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84893302342&doi=10.1039%2fc3cc48941h&partnerID=40&md5=39f546fbe247f3a35466bead3453213a
dc.subjectarticleen
dc.subjectunclassified drugen
dc.subjectsynthesisen
dc.subjectchemical structureen
dc.subjectstereoisomerismen
dc.subjectchiralityen
dc.subjectcyclopropanationen
dc.subjectenantiomeren
dc.subjectmalonic aciden
dc.subjectnuclear magnetic resonanceen
dc.subjectcarbon 13en
dc.subjectcyclo tris malonateen
dc.titleAn unexpected stereoisomerism in enantiomerically pure trisadducts of C60 with an inherently chiral trans-3,trans-3,trans-3 addition patternen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1039/c3cc48941h
dc.description.volume50
dc.description.issue16
dc.description.startingpage1995
dc.description.endingpage1998
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 :2</p>en
dc.source.abbreviationChem.Commun.en
dc.contributor.orcidChronakis, Nikos [0000-0002-2726-5290]
dc.gnosis.orcid0000-0002-2726-5290


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