Kozhushkov, Sergei I.

[["dc.bibliographiccitation.firstpage","142"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Organic & Biomolecular Chemistry"],["dc.bibliographiccitation.lastpage","148"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Deponti, Monica"],["dc.contributor.author","Kozhushkov, Sergei I."],["dc.contributor.author","Yufit, Dmitry S."],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T09:30:56Z"],["dc.date.available","2018-11-07T09:30:56Z"],["dc.date.issued","2013"],["dc.description.abstract","The chemical behavior of cyclopropyl-substituted alkynes has been probed using the reaction conditions of ruthenium-catalyzed oxidative C-H/O-H and C-H/N-H bond functionalizations. The oxidative annulations proceeded with complete conservation of all cyclopropane fragments and allowed for the one-step preparation of synthetically useful cyclopropyl-substituted isocoumarins and isoquinolones with high regioselectivities and chemical yields. The connectivities of the key heterocyclic products were unambiguously established by X-ray diffraction analysis."],["dc.description.sponsorship","Astra-Zeneca; EPSRC (UK)"],["dc.identifier.doi","10.1039/c2ob26250a"],["dc.identifier.isi","000311974300018"],["dc.identifier.pmid","23111695"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10175"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31428"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Royal Soc Chemistry"],["dc.relation.issn","1477-0520"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Ruthenium-catalyzed C-H/O-H and C-H/N-H bond functionalizations: oxidative annulations of cyclopropyl-substituted alkynes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2844"],["dc.bibliographiccitation.journal","Beilstein Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","2857"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","de Meijere, Armin"],["dc.contributor.author","Kozhushkov, Sergei I."],["dc.contributor.author","Yufit, Dmitry S."],["dc.contributor.author","Grosse, Christian"],["dc.contributor.author","Kaiser, Marcel"],["dc.contributor.author","Raev, Vitaly A."],["dc.date.accessioned","2018-11-07T09:31:31Z"],["dc.date.available","2018-11-07T09:31:31Z"],["dc.date.issued","2014"],["dc.description.abstract","Efficient and scalable syntheses of enantiomerically pure (2R,1'S,2'R)- and (2S,1'S,2'R)-3-[2-mono(di,tri)fluoromethylcyclopropyl]alanines 9a-c, as well as allo-D-threonine (4) and (2S,3R)-beta-methylphenylalanine (3), using the Belokon' approach with (S)- and (R)-2-[(N-benzylprolyl)amino]benzophenone [(S)- and (R)-10] as reusable chiral auxiliaries have been developed. Three new fluoromethyl analogues of the naturally occurring octadepsipeptide hormaomycin (1) with (fluoromethylcyclopropyl)alanine moieties have been synthesized and subjected to preliminary tests of their antibiotic activity."],["dc.description.sponsorship","Land Niedersachsen"],["dc.identifier.doi","10.3762/bjoc.10.302"],["dc.identifier.isi","000346467000001"],["dc.identifier.pmid","25550751"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/11913"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31547"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Beilstein-institut"],["dc.relation.issn","1860-5397"],["dc.rights","CC BY 2.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/2.0"],["dc.title","(2R,1 ' S,2 ' R)- and (2S,1 ' S,2 ' R)-3-[2-Mono(di,tri)fluoromethylcyclopropyl]alanines and their incorporation into hormaomycin analogues"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]