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| Manick AD, Salgues B, Parrain JL, et al. (2020) Access to Fluorenones Using Benzocyclopentynone Surrogate as Partner for the [2 + 2 + 2] Cycloaddition Reaction. Organic Letters. 22: 1894-1898 |
| Duarte L, Nag S, Castro M, et al. (2016) Chemical Sensors Based on New Polyamides Biobased on (Z) Octadec-9-Enedioic Acid and β-Cyclodextrin Macromolecular Chemistry and Physics. 217: 1620-1628 |
| Wang B, Zaborova E, Guieu S, et al. (2014) Site-selective hexa-hetero-functionalization of α-cyclodextrin an archetypical C₆-symmetric concave cycle. Nature Communications. 5: 5354 |
| Zaborova E, Guitet M, Prencipe G, et al. (2013) An "against the rules" double bank shot with diisobutylaluminum hydride to allow triple functionalization of α-cyclodextrin. Angewandte Chemie (International Ed. in English). 52: 639-44 |
| Zaborova E, Deschamp J, Guieu S, et al. (2011) Cavitand supported tetraphosphine: cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling. Chemical Communications (Cambridge, England). 47: 9206-8 |
| Guieu S, Zaborova E, Blériot Y, et al. (2010) Can hetero-polysubstituted cyclodextrins be considered as inherently chiral concave molecules? Angewandte Chemie (International Ed. in English). 49: 2314-8 |
| Zaborova E, Blériot Y, Sollogoub M. (2010) μ-Waves avoid large excesses of diisobutylaluminium-hydride (DIBAL-H) in the debenzylation of perbenzylated α-cyclodextrin Tetrahedron Letters. 51: 1254-1256 |
| Deunf E, Zaborova E, Guieu S, et al. (2010) Synthesis and electrochemical study of an original copper(II)-capped salen-cyclodextrin complex European Journal of Inorganic Chemistry. 4720-4727 |