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Chiral Diazaligands for Asymmetric Synthesis (Topics in Organometallic Chemistry)
 
 
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Chiral Diazaligands for Asymmetric Synthesis (Topics in Organometallic Chemistry) [Hardcover]

Marc Lemaire (Editor), Pierre Mangeney (Editor)

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Book Description

December 1, 2005 Topics in Organometallic Chemistry (Book 15)
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.

Editorial Reviews

Review

From the reviews: "Unlike most previous monologs on diazaligands, this book does not restrict itself to a specific class of dinitrogen compounds; instead, it covers the synthesis and utility of a broad range of chiral dinitrogen ligands, including saturated diamines and their derivatives, bisoxazolines, and salens. Due to the size of this field, this concise volume is not comprehensive. Rather, a collection of well-chosen topical overviews of the important elements in the chemistry of chiral diazaligands has been assembled. The inclusion of traditional as well as modern uses of diazaligands illustrates the developmental trajectory and future potential of the field." J. Am. Chem. Soc. 2006, 128, 9574 Maria C. Kozlowski, University of Pennsylvania

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Inside This Book (learn more)
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
dashes indicate results, glyoxal diimines, diaminocarbene complexes, oxidative kinetic resolution, nucleophilic allylic substitution, azomethine compounds, chiral ureas, azolium salts, successive reuses, chiral salen ligands, nitronate ion, aliphatic imines, solid phase immobilization, aromatic imines, cyclopropanation reaction, enantioselectivity results, achiral ligands, chiral bis, asymmetric cyclopropanation, syn diastereoselectivity, asymmetric catalysis, ethyl glyoxylate, chiral diamines, diastereoselective synthesis, poor enantioselectivities
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Chem Soc, Org Chem, Tetrahedron Lett, Org Lett, Chem Commun, Organomet Chem, Chem Rev, Mol Catal, Tetrahedron Asymmetry, Angew Chem Int Ed Engl, Berlin Heidelberg New York, Catal Lett, Bulman Page, Chem Eur, Med Chem, Springer-Verlag Berlin Heidelberg, Adv Synth Catal, Org Biomol Chem, Liquid Phase Immobilization, Non-covalently Immobilized Catalysts Based, Acta Chem Scand, Chem Ber, Fernández de la Pradilla, Inorg Chim Acta, Keywords Asymmetric
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