dc.creator | Matović, Radomir | |
dc.creator | Ivkovic, Aleksandar | |
dc.creator | Manojlović, Marija | |
dc.creator | Tokic-Vujosevic, Zorana | |
dc.creator | Saičić, Radomir N. | |
dc.date.accessioned | 2019-04-29T07:52:16Z | |
dc.date.available | 2019-04-29T07:52:16Z | |
dc.date.issued | 2006 | |
dc.identifier.issn | 0022-3263 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/2771 | |
dc.description.abstract | The combination of ring closing metathesis and beta-fragmentation offers an efficient entry into (Z)-configured medium ring cycloalkenes. The fragmentation step can be effected under anionic or radical conditions. The versatility of this method is demonstrated by the total synthesis of (+/-)-periplanone C - a macrocyclic pheromone of Periplaneta americana. | en |
dc.publisher | American Chemical Society (ACS) | |
dc.relation | info:eu-repo/grantAgreement/MESTD/MPN2006-2010/142021/RS// | |
dc.rights | restrictedAccess | |
dc.source | Journal of Organic Chemistry | |
dc.title | Ring closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone C | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Саичић, Радомир Н.; Токиц-Вујосевиц, Зорана; Манојловић, Марија; Ивковиц, Aлександар; Матовић, Радомир; | |
dc.citation.volume | 71 | |
dc.citation.issue | 25 | |
dc.citation.spage | 9411 | |
dc.citation.epage | 9419 | |
dc.citation.other | 71(25): 9411-9419 | |
dc.citation.rank | M21 | |
dc.identifier.pmid | 17137368 | |
dc.identifier.doi | 10.1021/jo061790j | |
dc.identifier.scopus | 2-s2.0-33845527881 | |
dc.identifier.wos | 000242426900019 | |
dc.type.version | publishedVersion | en |