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hal.structure.identifierPeoples Friendship University of Russia [RUDN University] [RUDN]
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorBERDNIKOVA, Daria V.
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorALIYEU, Tseimur M.
hal.structure.identifierLaboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
dc.contributor.authorDELBAERE, Stéphanie
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorFEDOROV, Yuri V.
hal.structure.identifierLaboratoire Ondes et Matière d'Aquitaine [LOMA]
dc.contributor.authorJONUSAUSKAS, Gediminas
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorNOVIKOV, Valentin V.
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorPAVLOV, Alexander A.
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorPEREGUDOV, Alexander S.
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorSHEPEL', Nikolay E.
hal.structure.identifierPeoples Friendship University of Russia [RUDN University] [RUDN]
dc.contributor.authorZUBKOV, Fedor I.
hal.structure.identifierA.N. Nismeyanov Institute of Organoelement Compounds
dc.contributor.authorFEDOROVA, Оlga A.
dc.date.created2016-10-27
dc.date.issued2017-04
dc.identifier.issn0143-7208
dc.description.abstractEnThe regio and stereoselective [2þ2] photocycloaddition of 15 crown 5 containing styrylheterocycles resulting in formation of only one cyclobutane isomer out of eleven possible is described. It was shown that the cycloaddition takes place solely in the case of the supramolecular preorganization of the reactive molecules provided by both p p stacking interaction of the heterocyclic fragments and sandwich type coordination of the crown ether residues by the barium cation. The results point out the importance of the supramolecular approach for the synthesis of cyclobutane derivatives with desired structure and conformation.
dc.language.isoen
dc.publisherElsevier
dc.rights.urihttp://creativecommons.org/licenses/by-sa/
dc.title.enRegio- and stereoselective [2+2] photocycloaddition in Ba2+ templated supramolecular dimers of styryl-derivatized aza-heterocycles
dc.typeArticle de revue
dc.identifier.doi10.1016/j.dyepig.2016.11.053
dc.subject.halPhysique [physics]/Physique [physics]/Chimie-Physique [physics.chem-ph]
bordeaux.journalDyes and Pigments
bordeaux.page397 - 402
bordeaux.volume139
bordeaux.peerReviewedoui
hal.identifierhal-01441885
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01441885v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Dyes%20and%20Pigments&rft.date=2017-04&rft.volume=139&rft.spage=397%20-%20402&rft.epage=397%20-%20402&rft.eissn=0143-7208&rft.issn=0143-7208&rft.au=BERDNIKOVA,%20Daria%20V.&ALIYEU,%20Tseimur%20M.&DELBAERE,%20St%C3%A9phanie&FEDOROV,%20Yuri%20V.&JONUSAUSKAS,%20Gediminas&rft.genre=article


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