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dc.creatorVulović, Bojan
dc.creatorTrmčić, Milena
dc.creatorMatović, Radomir
dc.creatorSaičić, Radomir N.
dc.date.accessioned2020-02-05T11:13:01Z
dc.date.available2020-02-05T11:13:01Z
dc.date.issued2019
dc.identifier.issn1523-7060
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/3819
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/3388
dc.description.abstractUnsaturated oxyallyl cations with a suitably positioned alkene bond undergo 5-exo-cyclization with the formation of vinylcyclopentane derivatives. Alkyne analogues provide allenes. The reaction proceeds with a moderate to excellent level of stereoselectivity and allows for asymmetric induction in the reaction with chiral substrate.en
dc.publisherAmerican Chemical Society (ACS)
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS//
dc.relationSerbian Academy of Sciences and Arts (Project No. F193)
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/256716/EU//
dc.rightsrestrictedAccess
dc.sourceOrganic Letters
dc.titleCyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formationen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractВуловић, Бојан; Саичић, Радомир; Матовић, Радомир; Трмчић, Милена;
dc.citation.volume21
dc.citation.issue23
dc.citation.spage9618
dc.citation.epage9621
dc.citation.rankaM21~
dc.identifier.doi10.1021/acs.orglett.9b03791
dc.identifier.scopus2-s2.0-85076326919
dc.identifier.wos000502163300071
dc.type.versionpublishedVersion


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