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dc.contributor.authorChronakis, Nikosen
dc.creatorChronakis, Nikosen
dc.date.accessioned2019-11-21T06:17:45Z
dc.date.available2019-11-21T06:17:45Z
dc.date.issued2014
dc.identifier.issn1477-0520
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55344
dc.description.abstractInherently chiral multi-adducts of [60]fullerene represent unique chiral molecular tectons featuring fascinating optoelectronic properties. Herein we discuss the most recent progress in the synthesis of enantiomerically pure bis- and trisadducts of C60with the inherently chiral trans-3 and all-trans-3 addition patterns utilizing cyclo-[n]-malonate tethers derived from (-)-dimethyl-2,3-O-isopropylidene-L-tartrate. Some future perspectives regarding the investigation of these chiral building blocks in modern areas of research are discussed. © The Royal Society of Chemistry 2014.en
dc.sourceOrganic and Biomolecular Chemistryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84908043085&doi=10.1039%2fc4ob01666a&partnerID=40&md5=66db0d04b6ab9390826990565fe7fc5c
dc.subjectL-tartaric acidsen
dc.subjectTris-adductsen
dc.titleThe journey of L-tartaric acid in the world of enantiomerically pure bis- and trisadducts of C60with the inherently chiral trans-3 and all-trans-3 addition patternsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1039/c4ob01666a
dc.description.volume12
dc.description.issue43
dc.description.startingpage8574
dc.description.endingpage8579
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.source.abbreviationOrg.Biomol.Chem.en
dc.contributor.orcidChronakis, Nikos [0000-0002-2726-5290]


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