Larionov, Oleg V.

[["dc.bibliographiccitation.issue","18"],["dc.bibliographiccitation.journal","ChemInform"],["dc.bibliographiccitation.volume","40"],["dc.contributor.author","Lygin, Alexander V."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2021-12-08T12:29:43Z"],["dc.date.available","2021-12-08T12:29:43Z"],["dc.date.issued","2009"],["dc.identifier.doi","10.1002/chin.200918119"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/96186"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.eissn","1522-2667"],["dc.relation.issn","0931-7597"],["dc.rights.uri","http://doi.wiley.com/10.1002/tdm_license_1.1"],["dc.title","ChemInform Abstract: Oligosubstituted Pyrroles Directly from Substituted Methyl Isocyanides and Acetylenes."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","6363"],["dc.bibliographiccitation.issue","31"],["dc.bibliographiccitation.journal","Organic & Biomolecular Chemistry"],["dc.bibliographiccitation.lastpage","6374"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","de Meijere, Armin"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Lygin, Alexander V."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Sokolov, Viktor V."],["dc.contributor.author","Graef, Tine"],["dc.contributor.author","Es-Sayed, Mazen"],["dc.date.accessioned","2018-11-07T09:15:11Z"],["dc.date.available","2018-11-07T09:15:11Z"],["dc.date.issued","2012"],["dc.description.abstract","Successful biochemical studies of the natural products belactosin A and C and their acylated congeners have shown a beta-lactonecarboxamide moiety to be a possible core structure of powerful proteasome inhibitors. As a part of further investigations, variously decorated simplified beta-lactonecarboxamides have been synthesized in order to understand structure-biological activity relations in detail, to find ways of improving their biological activity and stability and to reduce the complexity of their preparation. Biological tests showed that the best compounds possess a high potential against phytopathogenic fungi in the greenhouse."],["dc.identifier.doi","10.1039/c2ob25586c"],["dc.identifier.isi","000306480100015"],["dc.identifier.pmid","22735304"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10202"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/27613"],["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","Synthesis and biological activity of simplified belactosin C 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"]]

[["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","ChemInform"],["dc.bibliographiccitation.volume","38"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2021-12-08T12:29:33Z"],["dc.date.available","2021-12-08T12:29:33Z"],["dc.date.issued","2007"],["dc.identifier.doi","10.1002/chin.200712053"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/96119"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.eissn","1522-2667"],["dc.relation.issn","0931-7597"],["dc.rights.uri","http://doi.wiley.com/10.1002/tdm_license_1.1"],["dc.title","Cyclopropyl Building Blocks for Organic Synthesis. Part 128. Ln(OTf)3-Catalyzed Insertion of Aryl Isocyanides into the Cyclopropane Ring."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7504"],["dc.bibliographiccitation.issue","20"],["dc.bibliographiccitation.journal","The Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","7510"],["dc.bibliographiccitation.volume","72"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Hoftneister, Anja"],["dc.contributor.author","Magull, Joerg"],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2018-11-07T10:58:27Z"],["dc.date.available","2018-11-07T10:58:27Z"],["dc.date.issued","2007"],["dc.description.abstract","[GRAPHICS] GaCl3 has been found to efficiently catalyze the formal cycloadditions of diazene derivatives 6 onto 2-arylcyclopropane-1, 1-dicarboxylates 5, giving rise to the pyrazolidine derivatives 7. The insertion into the cyclopropane ring proceeds with complete regioselectivity to furnish 5-arylpyrazolidine-1,2,3,3-tetracarboxylates exclusively; however, the cis-configured azo compound N-phenyltriazolinedione gave the two possible regioisomeric pyrazolidine derivatives in ratios varying from 1:1.5 to 1:3. Conceivable mechanisms of these transformations are being discussed."],["dc.identifier.doi","10.1021/jo0704816"],["dc.identifier.isi","000249698200003"],["dc.identifier.pmid","17824644"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/50484"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0022-3263"],["dc.title","GaCl3-Catalyzed insertion of diazene derivatives into the cyclopropane ring"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","7791"],["dc.bibliographiccitation.issue","22"],["dc.bibliographiccitation.journal","Organic & Biomolecular Chemistry"],["dc.bibliographiccitation.lastpage","7798"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Ludwig, Antje"],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Lygin, Alexander V."],["dc.contributor.author","Groll, Michael"],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2018-11-07T09:01:51Z"],["dc.date.available","2018-11-07T09:01:51Z"],["dc.date.issued","2011"],["dc.description.abstract","Successful biochemical studies of the natural products belactosin A and C as well as their more stable acylated derivatives have proved them to be powerful proteasome inhibitors and thereby potential candidates as pharmacologically relevant active compounds. In order to understand their structure-biological activity relations in detail and to findways of improving their biological activity, four new modified belactosin congeners have been synthesized and tested. One of them (compound 6) turned out to be a more potent inhibitor against HeLa cells than the known proteasome inhibitor MG132."],["dc.description.sponsorship","Degussa Foundation (Evonik Industries AG)"],["dc.identifier.doi","10.1039/c1ob05661a"],["dc.identifier.isi","000296203700029"],["dc.identifier.pmid","21946808"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10465"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/24529"],["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","Synthesis and biological activity of optimized belactosin C congeners"],["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","3542"],["dc.bibliographiccitation.issue","21"],["dc.bibliographiccitation.journal","Synthesis"],["dc.bibliographiccitation.lastpage","3546"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2018-11-07T08:59:02Z"],["dc.date.available","2018-11-07T08:59:02Z"],["dc.date.issued","2006"],["dc.description.abstract","The insertion of two molecules of an aryl isocyanide into bisacceptor-activated cyclopropane derivatives has been observed for the first time. The reaction proceeds best under the catalysis of Pr(OTf)(3) and offers a facile access to the synthetically useful and potentially pharmacologically relevant substituted dialkyl 3-(arylamino)-2-(arylimino)cyclopent-3-ene-1,1-dicarboxylates in moderate yields (21-65%)."],["dc.identifier.doi","10.1055/s-2006-942514"],["dc.identifier.isi","000242403700003"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/23790"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Georg Thieme Verlag Kg"],["dc.relation.issn","0039-7881"],["dc.title","Ln(OTf)(3)-catalyzed insertion of aryl isocyanides into the cyclopropane ring"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","ChemInform"],["dc.bibliographiccitation.volume","39"],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Hofmeister, Anja"],["dc.contributor.author","Magull, Joerg"],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2021-12-08T12:29:38Z"],["dc.date.available","2021-12-08T12:29:38Z"],["dc.date.issued","2008"],["dc.identifier.doi","10.1002/chin.200806111"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/96151"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-476"],["dc.relation.eissn","1522-2667"],["dc.relation.issn","0931-7597"],["dc.rights.uri","http://doi.wiley.com/10.1002/tdm_license_1.1"],["dc.title","ChemInform Abstract: Cyclopropyl Building Blocks in Organic Synthesis. Part 141. GaCl3-Catalyzed Insertion of Diazene Derivatives into the Cyclopropane Ring."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","227"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Chemistry - A European Journal"],["dc.bibliographiccitation.lastpage","236"],["dc.bibliographiccitation.volume","15"],["dc.contributor.author","Lygin, Alexander V."],["dc.contributor.author","Larionov, Oleg V."],["dc.contributor.author","Korotkov, Vadim S."],["dc.contributor.author","de Meijere, Armin"],["dc.date.accessioned","2018-11-07T08:34:03Z"],["dc.date.available","2018-11-07T08:34:03Z"],["dc.date.issued","2009"],["dc.description.abstract","The formal cycloaddition of alpha-metallated methyl isocyanides 1 onto the triple bond of electron-deficient acetylenes 2 represents a direct and convenient approach to oligosubstituted pyrroles 3. The scope and limitations of this reaction (24 examples, 25-97% yield) are reported along with an optimization of the reaction conditions and a rationalization of the mechanism. in addition, it related newly developed Cu(1)-mediated synthesis of 2.3-disubstituted pyrrole by the reaction of copper acetylides derived from unactivated terminal alkynes with Substituted methyl isocyanides is described (11 examples, 5-88% yield)."],["dc.identifier.doi","10.1002/chem.200801395"],["dc.identifier.isi","000262301900027"],["dc.identifier.pmid","19025729"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/17728"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","0947-6539"],["dc.title","Oligosubstituted Pyrroles Directly from Substituted Methyl Isocyanides and Acetylenes"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]