Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine

dc.creator	Trajković, Milos
dc.creator	Balanac, Vesna
dc.creator	Ferjančić, Zorana
dc.creator	Saičić, Radomir
dc.date.accessioned	2018-11-22T00:29:33Z
dc.date.available	2018-11-22T00:29:33Z
dc.date.issued	2014
dc.identifier.issn	2046-2069
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/1876
dc.description.abstract	Enantioselective synthesis of (+)-swainsonine was achieved in 9 steps, with 24% overall yield. The key feature of the synthesis is the tactical combination of reactions: organocatalyzed aldolization/reductive amination, which allows for a rapid construction of highly functionalized heterocyclic systems. In a similar way (+)-8-epi-swainsonine was synthesized (7 steps, 28%).	en
dc.publisher	Royal Soc Chemistry, Cambridge
dc.relation	info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS//
dc.relation	Serbian Academy of Sciences and Arts [F193]
dc.rights	restrictedAccess
dc.source	RSC Advances
dc.title	Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine	en
dc.type	article
dc.rights.license	ARR
dcterms.abstract	Ферјанчић, Зорана; Трајковиц, Милос; Баланац, Весна; Саичић, Радомир;
dc.citation.volume	4
dc.citation.issue	96
dc.citation.spage	53722
dc.citation.epage	53724
dc.identifier.wos	000344468800042
dc.identifier.doi	10.1039/c4ra11978a
dc.citation.other	4(96): 53722-53724
dc.citation.rank	M21
dc.type.version	publishedVersion
dc.identifier.scopus	2-s2.0-84908409752