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dc.creatorMatović, Radomir
dc.creatorIvkovic, Aleksandar
dc.creatorManojlović, Marija
dc.creatorTokic-Vujosevic, Zorana
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-04-29T07:52:16Z
dc.date.available2019-04-29T07:52:16Z
dc.date.issued2006
dc.identifier.issn0022-3263
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2771
dc.description.abstractThe 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.publisherAmer Chemical Soc, Washington
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142021/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Organic Chemistry
dc.titleRing closing metathesis/fragmentation route to (Z)-configured medium ring cycloalkenes. Total synthesis of (+/-)-periplanone Cen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСаичић, Радомир Н.; Токиц-Вујосевиц, Зорана; Манојловић, Марија; Ивковиц, Aлександар; Матовић, Радомир;
dc.citation.volume71
dc.citation.issue25
dc.citation.spage9411
dc.citation.epage9419
dc.citation.other71(25): 9411-9419
dc.citation.rankM21
dc.identifier.pmid17137368
dc.identifier.doi10.1021/jo061790j
dc.identifier.rcubKon_1761
dc.identifier.scopus2-s2.0-33845527881
dc.identifier.wos000242426900019
dc.type.versionpublishedVersionen


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