Li, Jie

[["dc.bibliographiccitation.firstpage","3315"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","3318"],["dc.bibliographiccitation.volume","19"],["dc.contributor.author","Zhang, Z."],["dc.contributor.author","Han, Shengnan"],["dc.contributor.author","Tang, Mengyao"],["dc.contributor.author","Ackermann, Lutz"],["dc.contributor.author","Li, Jie"],["dc.date.accessioned","2018-11-07T10:22:39Z"],["dc.date.available","2018-11-07T10:22:39Z"],["dc.date.issued","2017"],["dc.description.abstract","Efficient cobalt(III)-catalyzed (hetero)aryl and alkenyl C-H hydroarylations of maleimides and maleate esters have been achieved under remarkably mild reaction conditions. Thus, the versatile cobalt(III) catalyst [Cp CoI2(CO)] showed excellent atom-and step-economy as well as high chemo- and site-selectivity providing expedient access to pharmacologically useful succinimides with wide functional group tolerance."],["dc.identifier.doi","10.1021/acs.orglett.7b01480"],["dc.identifier.isi","000403854300070"],["dc.identifier.pmid","28590740"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42314"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1523-7052"],["dc.relation.issn","1523-7060"],["dc.title","C-H Alkylations of (Hetero)Arenes by Maleimides and Maleate Esters through Cobalt(III) Catalysis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","664"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","The Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","672"],["dc.bibliographiccitation.volume","82"],["dc.contributor.author","Zhang, Z."],["dc.contributor.author","Tang, Mengyao"],["dc.contributor.author","Han, Shengnan"],["dc.contributor.author","Ackermann, Lutz"],["dc.contributor.author","Li, Jie"],["dc.date.accessioned","2018-11-07T10:28:28Z"],["dc.date.available","2018-11-07T10:28:28Z"],["dc.date.issued","2017"],["dc.description.abstract","Rhodium(III)-catalyzed C-H bond functionalization for the synthesis of beta-aryl aldehydes and ketones from (hetero)aryl oximes, pyri(mi)dine, as well as pyrazoles and alpha,beta-unsaturated carbonyl compounds has been developed under exceedingly mild reaction conditions. Thus, the versatile rhodium(III) catalysis features high step- and atom-economy, oxidant-free reaction conditions, and broad substrate scope."],["dc.identifier.doi","10.1021/acs.joc.6b02672"],["dc.identifier.isi","000391781900064"],["dc.identifier.pmid","27966963"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/43427"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","0022-3263"],["dc.title","Carboxylate-Enhanced Rhodium(III)-Catalyzed Aryl C-H Alkylation with Conjugated Alkenes under Mild Conditions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2742"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","2745"],["dc.bibliographiccitation.volume","18"],["dc.contributor.author","Li, Jie"],["dc.contributor.author","Tang, Mengyao"],["dc.contributor.author","Zang, Lei"],["dc.contributor.author","Zhang, X."],["dc.contributor.author","Zhang, Z."],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T10:12:54Z"],["dc.date.available","2018-11-07T10:12:54Z"],["dc.date.issued","2016"],["dc.description.abstract","A cobalt(III),-catalyzed C-H/N-H bond functionalization for the synthesis of 1-aniinoisoquincilines from aryl amidines and diazo compounds has been developed: The reaction proceeds under mild reaction conditions, obviates the need for oxidants, produces only N-2 and H2O as the byproducts, and features a broad substrate scope."],["dc.identifier.doi","10.1021/acs.orglett.6b01199"],["dc.identifier.isi","000377319000057"],["dc.identifier.pmid","27219713"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40328"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Chemical Soc"],["dc.relation.issn","1523-7052"],["dc.relation.issn","1523-7060"],["dc.title","Amidines for Versatile Cobalt(III)-Catalyzed Synthesis of Isoquinolines through C-H Functionalization with Diazo Compounds"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","660"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","European Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","664"],["dc.bibliographiccitation.volume","2019"],["dc.contributor.author","Tang, Mengyao"],["dc.contributor.author","Li, Yunpeng"],["dc.contributor.author","Han, Shengnan"],["dc.contributor.author","Liu, Lei"],["dc.contributor.author","Ackermann, Lutz"],["dc.contributor.author","Li, Jie"],["dc.date.accessioned","2020-12-10T14:06:28Z"],["dc.date.available","2020-12-10T14:06:28Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1002/ejoc.201801535"],["dc.identifier.issn","1434-193X"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/69910"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Rhodium(III)-Catalyzed C-H Alkylation/Nucleophilic Addition Domino Reaction"],["dc.title.alternative","Rhodium(III)-Catalyzed C-H Alkylation/Nucleophilic Addition Domino Reaction"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]