Search Results - "Radhoff, Niklas"

1,4-Aryl migration in ketene-derived enolates by a polar-radical-crossover cascade by Radhoff, Niklas, Studer, Armido

“…The arylation of carboxylic acid derivatives via Smiles rearrangement has gained great interest in recent years. Both radical and ionic approaches, as well as…”
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Functionalization of α‐C(sp3)−H Bonds in Amides Using Radical Translocating Arylating Groups by Radhoff, Niklas, Studer, Armido

“…α‐C−H arylation of N‐alkylamides using 2‐iodoarylsulfonyl radical translocating arylating (RTA) groups is reported. The method allows the construction of…”
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Oxindole synthesis via polar-radical crossover of ketene-derived amide enolates in a formal [3 + 2] cycloaddition by Radhoff, Niklas, Studer, Armido

“…Herein we introduce a simple, efficient and transition-metal free method for the preparation of valuable and sterically hindered 3,3-disubstituted oxindoles…”
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Oxindole synthesis via polar-radical crossover of ketene-derived amide enolates in a formal 3 + 2 cycloaddition by Radhoff, Niklas, Studer, Armido

“…Herein we introduce a simple, efficient and transition-metal free method for the preparation of valuable and sterically hindered 3,3-disubstituted oxindoles…”
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Lewis Acid Catalyzed Formal (3+2)‐Cycloaddition of Bicyclobutanes with Ketenes by Radhoff, Niklas, Daniliuc, Constantin G, Studer, Armido

“…Design, synthesis and application of benzene bioisosteres have attracted a lot of attention in the past 20 years. Recently, bicyclo[2.1.1]hexanes have emerged…”
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Lewis Acid Catalyzed Formal (3+2)‐Cycloaddition of Bicyclo[1.1.0]butanes with Ketenes by Radhoff, Niklas, Daniliuc, Constantin G., Studer, Armido

“…Design, synthesis and application of benzene bioisosteres have attracted a lot of attention in the past 20 years. Recently, bicyclo[2.1.1]hexanes have emerged…”
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Radikalische Funktionalisierung von α‐C(sp3)‐H‐Bindungen in Amiden durch Translokations‐induzierende arylierende Gruppen by Radhoff, Niklas, Studer, Armido

“…Die radikalische α‐C‐H‐Arylierung in N‐Alkylamiden durch Translokations‐induzierende arylierende (RTA) Gruppen auf Basis von 2‐Iodarylsulfonylchloriden wird…”
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Lewis‐Säure‐katalysierte formale (3+2)‐Cycloaddition von Bicyclo[1.1.0]butanen mit Ketenen by Radhoff, Niklas, Daniliuc, Constantin G., Studer, Armido

“…Design, Synthese und Anwendung von Benzolbioisosteren haben in den letzten 20 Jahren viel Aufmerksamkeit erfahren. In jüngster Zeit haben sich…”
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Lewis‐Säure‐katalysierte formale (3+2)‐Cycloaddition von Bicyclobutanen mit Ketenen by Radhoff, Niklas, Daniliuc, Constantin G, Studer, Armido

“…Design, Synthese und Anwendung von Benzolbioisosteren haben in den letzten 20 Jahren viel Aufmerksamkeit erfahren. In jüngster Zeit haben sich…”
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Oxindole synthesis polar-radical crossover of ketene-derived amide enolates in a formal [3 + 2] cycloaddition by Radhoff, Niklas, Studer, Armido

“…Herein we introduce a simple, efficient and transition-metal free method for the preparation of valuable and sterically hindered 3,3-disubstituted oxindoles…”
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Radikalische Funktionalisierung von α‐C(sp3)‐H‐Bindungen in Amiden durch Translokations‐induzierende arylierende Gruppen by Radhoff, Niklas, Studer, Armido

“…Die radikalische α‐C‐H‐Arylierung in N‐Alkylamiden durch Translokations‐induzierende arylierende (RTA) Gruppen auf Basis von 2‐Iodarylsulfonylchloriden wird…”
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