- Alternative title
-
Selen-vermittelte Allenylierung und Allylierungsreaktionen von N- und O-Nukleophilen
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Regensburg, Universität Regensburg, Dissertation, 2024
- Keyword
-
Chemische Synthese
Organische Synthese
- Event
-
Veröffentlichung
- (where)
-
Regensburg
- (who)
-
Universitätsbibliothek Regensburg
- (when)
-
2024
- Creator
- Contributor
-
Breder, Alexander
- URN
-
urn:nbn:de:bvb:355-epub-582018
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2225, 2:10 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Ramadas Narasimhamurthy, Poorva
- Breder, Alexander
- Universitätsbibliothek Regensburg
Time of origin
- 2024
Other Objects (12)
Enantioselective nickel-catalyzed anodic oxidative dienylation and allylation reactions
Reactions of p-Benzoquinone with Sulfur Nucleophiles
New reactions with arynes and allylation nitrosoarenes with chiral allylboronates
Lewis base catalyzed reactions with latent nucleophiles and phosphonium intermediates
Tunable Gold‐catalyzed Reactions of Propargyl Alcohols and Aryl Nucleophiles
Observation of unusual outer-sphere mechanism using simple alkenes as nucleophiles in allylation chemistry
Investigation of differently substituted allylboronic esters in allylation reactions
Reactivity selectivity relationships in reactions of carbocations with nucleophiles
Enantio- and Diastereoselective α-Allylation
Molecular diversity of the reactions of MBH carbonates of isatins and various nucleophiles
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
Enantioselective nickel-catalyzed anodic oxidative dienylation and allylation reactions
Reactions of p-Benzoquinone with Sulfur Nucleophiles
New reactions with arynes and allylation nitrosoarenes with chiral allylboronates
Lewis base catalyzed reactions with latent nucleophiles and phosphonium intermediates
Tunable Gold‐catalyzed Reactions of Propargyl Alcohols and Aryl Nucleophiles
Observation of unusual outer-sphere mechanism using simple alkenes as nucleophiles in allylation chemistry
Investigation of differently substituted allylboronic esters in allylation reactions
Reactivity selectivity relationships in reactions of carbocations with nucleophiles
Enantio- and Diastereoselective α-Allylation
Molecular diversity of the reactions of MBH carbonates of isatins and various nucleophiles
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules
Enantioselective nickel-catalyzed anodic oxidative dienylation and allylation reactions
Reactions of p-Benzoquinone with Sulfur Nucleophiles
New reactions with arynes and allylation nitrosoarenes with chiral allylboronates
Lewis base catalyzed reactions with latent nucleophiles and phosphonium intermediates
Tunable Gold‐catalyzed Reactions of Propargyl Alcohols and Aryl Nucleophiles
Observation of unusual outer-sphere mechanism using simple alkenes as nucleophiles in allylation chemistry
Investigation of differently substituted allylboronic esters in allylation reactions
Reactivity selectivity relationships in reactions of carbocations with nucleophiles
Enantio- and Diastereoselective α-Allylation
Molecular diversity of the reactions of MBH carbonates of isatins and various nucleophiles
Allylation of C ‐, N ‐, and O ‐Nucleophiles via a Mechanochemically‐Driven Tsuji–Trost Reaction Suitable for Late‐Stage Modification of Bioactive Molecules