Prikaz osnovnih podataka o dokumentu
Intermolecular free radical additions to strained cycloalkenes. Cyclopropene and cyclobutene as radical accepters
dc.creator | Ferjančić, Zorana | |
dc.creator | Čeković, Živorad | |
dc.creator | Saičić, Radomir | |
dc.date.accessioned | 2018-11-22T00:03:11Z | |
dc.date.available | 2018-11-22T00:03:11Z | |
dc.date.issued | 2000 | |
dc.identifier.issn | 0040-4039 | |
dc.identifier.uri | https://cherry.chem.bg.ac.rs/handle/123456789/433 | |
dc.description.abstract | Intermolecular additions of electrophilic radicals to cyclopropene and cyclobutene derivatives afford the addition products in 37-50% yield. The strain relief in the intermediary radical accelerates the addition, as shown by competitive addition experiments. (C) 2000 Elsevier Science Ltd. All rights reserved. | en |
dc.publisher | Pergamon-Elsevier Science Ltd, Oxford | |
dc.rights | restrictedAccess | |
dc.source | Tetrahedron Letters | |
dc.subject | radicals and radical reactions | en |
dc.subject | cyclopropenes | en |
dc.subject | cyclobutenes | en |
dc.subject | xanthates | en |
dc.subject | strained compounds | en |
dc.title | Intermolecular free radical additions to strained cycloalkenes. Cyclopropene and cyclobutene as radical accepters | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Саичић, Радомир; Цековиц, З; Ферјанчић, Зорана; | |
dc.citation.volume | 41 | |
dc.citation.issue | 16 | |
dc.citation.spage | 2979 | |
dc.citation.epage | 2982 | |
dc.identifier.wos | 000086681200050 | |
dc.identifier.doi | 10.1016/S0040-4039(00)00286-0 | |
dc.citation.other | 41(16): 2979-2982 | |
dc.citation.rank | M21 | |
dc.type.version | publishedVersion | en |
dc.identifier.scopus | 2-s2.0-0342369341 |