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dc.contributor.authorChronakis, Nikosen
dc.contributor.authorOrfanopoulos, Michaelen
dc.creatorChronakis, Nikosen
dc.creatorOrfanopoulos, Michaelen
dc.date.accessioned2019-11-21T06:17:48Z
dc.date.available2019-11-21T06:17:48Z
dc.date.issued1999
dc.identifier.issn1523-7060
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55352
dc.description.abstract(Matrix Presented) The ene reaction of arylallyl alkenes with C60 occurs either by a concerted mechanism or by the reversible formation of a charged or a dipolar intermediate, followed by the C-H(D) breakage in a rate-limiting step.en
dc.sourceOrganic lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0006115654&partnerID=40&md5=f8963c90dcb4f77160620d79031d5d2a
dc.titleEne Reaction of Arylallyl Alkenes with C60. A Mechanistic Approachen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume1
dc.description.issue12
dc.description.startingpage1909
dc.description.endingpage1912
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 :5</p>en
dc.source.abbreviationOrg.Lett.en
dc.contributor.orcidChronakis, Nikos [0000-0002-2726-5290]
dc.contributor.orcidOrfanopoulos, Michael [0000-0002-7785-2071]
dc.gnosis.orcid0000-0002-2726-5290
dc.gnosis.orcid0000-0002-7785-2071


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