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Ernst-Ulrich Würthwein (1948-)

Chemiker

Name	Ernst-Ulrich Würthwein
Zeit	1948- (Lebensdaten)
Ort	Tübingen (Geburtsort) Deutschland
Beruf	Chemiker (charakteristischer Beruf)
Datensatztyp	Person
GND-Nummer	172467519
Datensatz-ID	172467519
Beteiligt an alle anzeigen The Boekelheide Rearrangement of Pyrimidine N ‐oxides as a Case Study of Closed or Open Shell Reactions ‐ Experimental and Computational Evidence for the Participation of Radical Intermediates Semisynthetic Approach toward Biologically Active Derivatives of Phenylspirodrimanes from S. chartarum Alkoxyallene‐Based LANCA Three‐Component Synthesis of 1,2‐Diketones, Quinoxalines, and Unique Isoindenone Dimers and a Computational Study of the Isoindenone Dimerization Reactions of Al‐N Based Active Lewis Pairs with Ketones and 1,2‐Diketones: Insertion into Al‐N Bonds, C‐C and C‐N Bond Formation and a Tricyclic Saturated Tetraaza Compound New Reactivity Patterns in 3H‐Phosphaallene Chemistry (Aryl‐P=C=C (H)‐ t Bu): Hydroboration of the C=C Bond, Deprotonation and Trimerisation The (4+2)‐Cycloaddition of α‐Nitrosoalkenes with Thiochalcones as a Prototype of Periselective Hetero‐Diels–Alder Reactions—Experimental and Computational Studies Silyldefluorination of Fluoroarenes by Concerted Nucleophilic Aromatic Substitution Silyldefluorination of Fluoroarenes by Concerted Nucleophilic Aromatic Substitution Cooperative Activation of Isocyanates by Al–N‐Based Active Lewis Pairs and the Generation of a C 5 Chain by Simultaneous Formation of Two C–C Bonds Radikalische Hydrodehalogenierung von Arylbromiden und ‐chloriden mit Natriumhydrid und 1,4‐Dioxan Radical Hydrodehalogenation of Aryl Bromides and Chlorides with Sodium Hydride and 1,4‐Dioxane Struktur, Synthese und Eigenschaften von 2-Aza-allenium-Salzen [Aza-allenium-Salzen] Darstellung, Eigenschaften und Reaktionen von Adamantyl[malondialdehyden] tert.-Butyl[malondialdehyden] und Alkylidenmalondialdehyden

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Ernst-Ulrich Würthwein (1948-)

The Boekelheide Rearrangement of Pyrimidine N ‐oxides as a Case Study of Closed or Open Shell Reactions ‐ Experimental and Computational Evidence for the Participation of Radical Intermediates

Semisynthetic Approach toward Biologically Active Derivatives of Phenylspirodrimanes from S. chartarum

Alkoxyallene‐Based LANCA Three‐Component Synthesis of 1,2‐Diketones, Quinoxalines, and Unique Isoindenone Dimers and a Computational Study of the Isoindenone Dimerization

Reactions of Al‐N Based Active Lewis Pairs with Ketones and 1,2‐Diketones: Insertion into Al‐N Bonds, C‐C and C‐N Bond Formation and a Tricyclic Saturated Tetraaza Compound

New Reactivity Patterns in 3H‐Phosphaallene Chemistry (Aryl‐P=C=C (H)‐ t Bu): Hydroboration of the C=C Bond, Deprotonation and Trimerisation

The (4+2)‐Cycloaddition of α‐Nitrosoalkenes with Thiochalcones as a Prototype of Periselective Hetero‐Diels–Alder Reactions—Experimental and Computational Studies

Silyldefluorination of Fluoroarenes by Concerted Nucleophilic Aromatic Substitution

Silyldefluorination of Fluoroarenes by Concerted Nucleophilic Aromatic Substitution

Cooperative Activation of Isocyanates by Al–N‐Based Active Lewis Pairs and the Generation of a C 5 Chain by Simultaneous Formation of Two C–C Bonds

Radikalische Hydrodehalogenierung von Arylbromiden und ‐chloriden mit Natriumhydrid und 1,4‐Dioxan

Radical Hydrodehalogenation of Aryl Bromides and Chlorides with Sodium Hydride and 1,4‐Dioxane

Struktur, Synthese und Eigenschaften von 2-Aza-allenium-Salzen [Aza-allenium-Salzen]

Darstellung, Eigenschaften und Reaktionen von Adamantyl[malondialdehyden] tert.-Butyl[malondialdehyden] und Alkylidenmalondialdehyden