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Chiral diazaligands for asymmetric synthesis
The use of phosphine derivatives has historically induced the tremendous development of catalysis (both non-asymmetric and asymmetric). Although the chemistry of amines is more documented, the use of nitrogen-containing ligands only appeared recently. Nevertheless, during the last ten years, the res...
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| Auteurs principaux : | , |
|---|---|
| Format : | Livre |
| Langue : | anglais |
| Titre complet : | Chiral diazaligands for asymmetric synthesis / edited by Marc Lemaire, Pierre Mangeney |
| Édition : | 1st ed. 2005. |
| Publié : |
Berlin, Heidelberg :
Springer Berlin Heidelberg
, [20..] Cham : Springer Nature |
| Collection : | Topics in organometallic chemistry (Internet) ; 15 |
| Accès en ligne : |
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| Condition d'utilisation et de reproduction : | Conditions particulières de réutilisation pour les bénéficiaires des licences nationales : https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 |
| Contenu : | D. Savoia: Progresses in the Asymmetric Synthesis of 1,2-Diamines from Azomethine Compounds. O. Chuzel, O. Riant: Sparteine as a Chiral Ligand for Asymmetric Catalysis. E. Schulz: Use of N,N-Coordinating Ligands in Catalytic Asymmetric C-C Bond Formations: Example of Cyclopropanation, Diels-Alder Reaction, Nucleophilic Allylic Substitution. J.M. Fraile, J.I. García and J.A. Mayoral: Non-Covalent Immobilization of Catalysts based on Chiral Diazaligands. S. Roland, P. Mangeney: Chiral Diaminocarbene Complexes, Synthesis and Application in Asymmetric Catalysis. J.A.J. Breuzard, M.Lorraine Christ-Tommasino and M. Lemaire: Chiral Ureas and Thioureas in Asymmetric Catalysis. M. Fontecave, O. Hamelin and S. Ménage: Chiral-at-Metal Complexes as Asymmetric Catalysts |
| Sujets : | |
| Documents associés : | Autre format:
Chiral diazaligands for asymmetric synthesis Autre format: Chiral Diazaligands for Asymmetric Synthesis Autre format: Chiral Diazaligands for Asymmetric Synthesis Autre format: Chiral diazaligands for asymmetric synthesis |
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| 200 | 1 | |a Chiral diazaligands for asymmetric synthesis |f edited by Marc Lemaire, Pierre Mangeney | |
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| 225 | 0 | |a Topics in Organometallic Chemistry |x 1616-8534 |v 15 | |
| 327 | 1 | |a D. Savoia: Progresses in the Asymmetric Synthesis of 1,2-Diamines from Azomethine Compounds |a O. Chuzel, O. Riant: Sparteine as a Chiral Ligand for Asymmetric Catalysis |a E. Schulz: Use of N,N-Coordinating Ligands in Catalytic Asymmetric C-C Bond Formations: Example of Cyclopropanation, Diels-Alder Reaction, Nucleophilic Allylic Substitution |a J.M. Fraile, J.I. García and J.A. Mayoral: Non-Covalent Immobilization of Catalysts based on Chiral Diazaligands |a S. Roland, P. Mangeney: Chiral Diaminocarbene Complexes, Synthesis and Application in Asymmetric Catalysis |a J.A.J. Breuzard, M.Lorraine Christ-Tommasino and M. Lemaire: Chiral Ureas and Thioureas in Asymmetric Catalysis |a M. Fontecave, O. Hamelin and S. Ménage: Chiral-at-Metal Complexes as Asymmetric Catalysts | |
| 330 | |a The use of phosphine derivatives has historically induced the tremendous development of catalysis (both non-asymmetric and asymmetric). Although the chemistry of amines is more documented, the use of nitrogen-containing ligands only appeared recently. Nevertheless, during the last ten years, the results describing chiral diamine preparations and their uses in asymmetric catalysis and synthesis are increasing faster than their phosphorus counterparts. The reader will find in this volume the most recent methods for the synthesis of chiral diamines as well as their applications in asymmetric catalysis of CC bond formation. Particular attention will be given to spartein and derivatives of such diamines. Recently, the particular properties and the chemistry of amines allowed to obtain catalysts easy to separate and recycle and new types of ligands such as diaminocarbenes, ureas and thioureas. Finally, the complexing properties of some diamines allowed the formation of complexes with chirality "at the metal " which is of major theoretical interest and presents numerous potential applications | ||
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