Bis (Aluminyl) Magnesium: a Source of Nucleophilic or Radical Aluminium‐Centred Reactivity
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Bis (Aluminyl) Magnesium: a Source of Nucleophilic or Radical Aluminium‐Centred Reactivity ; day:22 ; month:04 ; year:2024 ; extent:7
Angewandte Chemie / International edition. International edition ; (22.04.2024) (gesamt 7)
- Creator
-
Griffin, Liam P.
Ellwanger, Mathias A.
Clark, Jonathon
Myers, William K.
Roper, Aisling F.
Heilmann, Andreas
Aldridge, Simon
- DOI
-
10.1002/anie.202405053
- URN
-
urn:nbn:de:101:1-2404231404211.179289154674
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:54 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
- Griffin, Liam P.
- Ellwanger, Mathias A.
- Clark, Jonathon
- Myers, William K.
- Roper, Aisling F.
- Heilmann, Andreas
- Aldridge, Simon
Other Objects (12)
Bis (Aluminyl) Magnesium: a Source of Nucleophilic or Radical Aluminium‐Centred Reactivity
Reactivity parameters for understanding nucleophilic organocatalysis
Reactivity parameters for understanding nucleophilic organocatalysis
Nucleophilic Triphenylgermanides of Magnesium and Calcium
Enabling nucleophilic reactivity in molecular calcium fluoride complexes
Nucleophilic reactivity of a copper(II)-hydroperoxo complex
Nucleophilic properties of purine bases: inherent reactivity versus reaction conditions
Nucleophilic Functionalization of a Cationic Pentaphosphole Complex–A Systematic Study of Reactivity
Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate
Structural and ion-pairing effects on the nucleophilic reactivity of carbanions and organometallics
Metal Enolates – Enamines – Enol Ethers: How Do Enolate Equivalents Differ in Nucleophilic Reactivity?
The atmospheric reactivity of the NO3 radical
Bis (Aluminyl) Magnesium: a Source of Nucleophilic or Radical Aluminium‐Centred Reactivity
Reactivity parameters for understanding nucleophilic organocatalysis
Reactivity parameters for understanding nucleophilic organocatalysis
Nucleophilic Triphenylgermanides of Magnesium and Calcium
Enabling nucleophilic reactivity in molecular calcium fluoride complexes
Nucleophilic reactivity of a copper(II)-hydroperoxo complex
Nucleophilic properties of purine bases: inherent reactivity versus reaction conditions
Nucleophilic Functionalization of a Cationic Pentaphosphole Complex–A Systematic Study of Reactivity
Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate
Structural and ion-pairing effects on the nucleophilic reactivity of carbanions and organometallics
Metal Enolates – Enamines – Enol Ethers: How Do Enolate Equivalents Differ in Nucleophilic Reactivity?
The atmospheric reactivity of the NO3 radical
Bis (Aluminyl) Magnesium: a Source of Nucleophilic or Radical Aluminium‐Centred Reactivity
Reactivity parameters for understanding nucleophilic organocatalysis
Reactivity parameters for understanding nucleophilic organocatalysis
Nucleophilic Triphenylgermanides of Magnesium and Calcium
Enabling nucleophilic reactivity in molecular calcium fluoride complexes
Nucleophilic reactivity of a copper(II)-hydroperoxo complex
Nucleophilic properties of purine bases: inherent reactivity versus reaction conditions
Nucleophilic Functionalization of a Cationic Pentaphosphole Complex–A Systematic Study of Reactivity
Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate
Structural and ion-pairing effects on the nucleophilic reactivity of carbanions and organometallics
Metal Enolates – Enamines – Enol Ethers: How Do Enolate Equivalents Differ in Nucleophilic Reactivity?