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.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","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"]]