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dc.creatorBjelaković, Mira
dc.creatorTodorović, Nina
dc.creatorMilić, Dragana
dc.date.accessioned2019-01-30T17:32:38Z
dc.date.available2019-01-30T17:32:38Z
dc.date.issued2012
dc.identifier.issn1434-193X
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/1106
dc.description.abstractTwo sets of new peptides incorporating fulleropyrrolidine units Fp-GABAn-Glym-OtBu have been designed, synthesized and completely characterized. In the first series the chain contained only GABA (?-aminobutyric) residues, whereas in the second one glycine moieties were also inserted as well as GABA. Most of the target compounds were prepared by DCC/DMAP-assisted coupling of previously synthesized GABA-containing fulleropyrrolidinic acid and corresponding C-protected small peptides, although for two fulleropeptides [3+2] cycloadditions of azomethine ylides to C60 were employed. All new compounds were characterized by standard spectroscopic methods. Complete assignments of peptide spin systems were achieved by extensive NMR analysis (1H, 13C, H,H-COSY, HSQC, HMBC and TOCSY).en
dc.publisherWiley-V C H Verlag Gmbh, Weinheim
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172002/RS//
dc.rightsrestrictedAccess
dc.sourceEuropean Journal of Organic Chemistry
dc.subjectSynthetic methodsen
dc.subjectPeptidomimeticsen
dc.subjectFullerenesen
dc.subjectFulleropeptidesen
dc.subjectNano particlesen
dc.titleAn Approach to Nanobioparticles - Synthesis and Characterization of Fulleropeptidesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractТодоровић, Нина; Бјелаковић, Мира; Милиц, Драгана;
dc.citation.issue27
dc.citation.spage5291
dc.citation.epage5300
dc.citation.other(27): 5291-5300
dc.citation.rankM21
dc.identifier.doi10.1002/ejoc.201200274
dc.identifier.rcubConv_2843
dc.identifier.scopus2-s2.0-84866260060
dc.identifier.wos000308580800020
dc.type.versionpublishedVersion


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