dc.creator | Vulović, Bojan | |
dc.creator | Trmčić, Milena | |
dc.creator | Matović, Radomir | |
dc.creator | Saičić, Radomir N. | |
dc.date.accessioned | 2020-02-05T11:13:01Z | |
dc.date.available | 2020-02-05T11:13:01Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1523-7060 | |
dc.identifier.uri | http://cherry.chem.bg.ac.rs/handle/123456789/3819 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/3388 | |
dc.description.abstract | Unsaturated 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.publisher | American Chemical Society (ACS) | |
dc.relation | info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS// | |
dc.relation | Serbian Academy of Sciences and Arts (Project No. F193) | |
dc.relation | info:eu-repo/grantAgreement/EC/FP7/256716/EU// | |
dc.rights | restrictedAccess | |
dc.source | Organic Letters | |
dc.title | Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Вуловић, Бојан; Саичић, Радомир; Матовић, Радомир; Трмчић, Милена; | |
dc.citation.volume | 21 | |
dc.citation.issue | 23 | |
dc.citation.spage | 9618 | |
dc.citation.epage | 9621 | |
dc.citation.rank | aM21~ | |
dc.identifier.doi | 10.1021/acs.orglett.9b03791 | |
dc.identifier.scopus | 2-s2.0-85076326919 | |
dc.identifier.wos | 000502163300071 | |
dc.type.version | publishedVersion | |