2 recherche sur le tag 'METAL CATALYSIS'   

Catalysis by metals: les Houches School, March 19-29, 1996 / Albert Jean Renouprez

Public ISBD Titre : Catalysis by metals: les Houches School, March 19-29, 1996 Type de document : texte imprimé Auteurs : Albert Jean Renouprez, Éditeur scientifique ; Hervé Jobic, Éditeur scientifique Editeur : Les Ulis : Les Editions de Physique Année de publication : 1997 Autre Editeur : Berlin : Springer Collection : Centre de Physique des Houches num. 6 Importance : xv, 221 p. Format : 24 cm ISBN/ISSN/EAN : 978-3-540-63708-0 Langues : Anglais (eng) Tags : METAL CATALYSIS  CATALYSIS  METALS Index. décimale : EQ -Equipe- Résumé : "This book presents the contributions from the winter school held at the Ecole de Physique des Houches in March 1996. They portray an evolution in catalysis by metals in several directions. The first domain is cooperation on emulation between theoretical chemistry and solid state physics leading to predictions of the reactivity of catalytic systems. The second domain which has become of primary importance is the abatement of pollution. The major achievement of catalysis in the past 10 years is the valorization of agricultural supplies. The book is a must for those who are concerned with catalysis, metals, physical techniques and catalyst reaction." Cote : LCC/L Num_Inv : 1780 Catalysis by metals: les Houches School, March 19-29, 1996 [texte imprimé] / Albert Jean Renouprez, Éditeur scientifique ; Hervé Jobic, Éditeur scientifique . - Les Ulis : Les Editions de Physique : Berlin : Springer, 1997 . - xv, 221 p. ; 24 cm. - (Centre de Physique des Houches; 6) . ISBN : 978-3-540-63708-0 Langues : Anglais (eng) Tags : METAL CATALYSIS  CATALYSIS  METALS Index. décimale : EQ -Equipe- Résumé : "This book presents the contributions from the winter school held at the Ecole de Physique des Houches in March 1996. They portray an evolution in catalysis by metals in several directions. The first domain is cooperation on emulation between theoretical chemistry and solid state physics leading to predictions of the reactivity of catalytic systems. The second domain which has become of primary importance is the abatement of pollution. The major achievement of catalysis in the past 10 years is the valorization of agricultural supplies. The book is a must for those who are concerned with catalysis, metals, physical techniques and catalyst reaction." Cote : LCC/L Num_Inv : 1780

Exemplaires(1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
1780	LCC/L	Texte imprimé	Equipe	Livre	Equipe - Demande préalable Disponible

Copper-catalyzed amination of aryl and alkenyl electrophiles / Shaughnessy, Kevin H.

Public ISBD Titre : Copper-catalyzed amination of aryl and alkenyl electrophiles Type de document : texte imprimé Auteurs : Shaughnessy, Kevin H., Auteur ; Ciganek, Engelbert, Auteur ; DeVasher, Rebecca, B., Auteur Editeur : Wiley-VCH Verlag Année de publication : 2017 Importance : ix, 679 p. ISBN/ISSN/EAN : 978-1-119-34598-5 Note générale : The contents of the book are taken from the comprehensive review of the topic in the Organic Reactions series. Optimal experimental conditions for the amination of aryl and alkenyl halides with all classes of nitrogen nucleophiles are presented. Specific experimental procedures from the literature are provided for the major classes of copper-catalyzed C?N coupling reactions. A tabular survey of all examples of Cu-catalyzed arylation and alkenylation of nitrogen nucleophiles is presented in 35 tables organized by nitrogen nucleophile and electrophilic coupling partner. Langues : Anglais (eng) Catégories : Catalyse Tags : METAL CATALYSIS  CATALYSIS Index. décimale : B-E Résumé : The metal-catalyzed amination of aryl and alkenyl electrophiles has developed into a widely used methodology for the synthesis of natural products, active pharmaceutical ingredients, agricultural chemicals, and materials for molecular electronics. Copper catalysts promote the coupling of a wide range of nitrogen nucleophiles, including amines, amides, and heteroaromatic nitrogen compounds with aryl and alkenyl halides. The reactivity profile of copper catalysts is complementary to that of palladium catalysts in many cases. Copper catalysts are highly effective with less nucleophilic nitrogen nucleophiles, such as amides and azoles, whereas palladium catalysts are more effective with more nucleophilic amine nucleophiles. Copper is an attractive alternative to palladium due to its significantly lower cost. In addition, high activity palladium catalysts require expensive and often air-sensitive ligands, whereas the modern copper systems use relatively stable and inexpensive diamine or amino acid ligands. Copper-catalyzed C?N coupling reactions are tolerant of a wide range of functional groups and have been applied to the synthesis of a variety of complex natural products. Significant work has also been done to understand the mechanism of these reactions. Current mechanistic understanding of these methodologies is covered in this monograph. Note de contenu : " Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles". Cote : B-E094 Num_Inv : 3558 Localisation : LCC (SdS) Copper-catalyzed amination of aryl and alkenyl electrophiles [texte imprimé] / Shaughnessy, Kevin H., Auteur ; Ciganek, Engelbert, Auteur ; DeVasher, Rebecca, B., Auteur . - Wiley-VCH Verlag, 2017 . - ix, 679 p. ISBN : 978-1-119-34598-5 The contents of the book are taken from the comprehensive review of the topic in the Organic Reactions series. Optimal experimental conditions for the amination of aryl and alkenyl halides with all classes of nitrogen nucleophiles are presented. Specific experimental procedures from the literature are provided for the major classes of copper-catalyzed C?N coupling reactions. A tabular survey of all examples of Cu-catalyzed arylation and alkenylation of nitrogen nucleophiles is presented in 35 tables organized by nitrogen nucleophile and electrophilic coupling partner. Langues : Anglais (eng) Catégories : Catalyse Tags : METAL CATALYSIS  CATALYSIS Index. décimale : B-E Résumé : The metal-catalyzed amination of aryl and alkenyl electrophiles has developed into a widely used methodology for the synthesis of natural products, active pharmaceutical ingredients, agricultural chemicals, and materials for molecular electronics. Copper catalysts promote the coupling of a wide range of nitrogen nucleophiles, including amines, amides, and heteroaromatic nitrogen compounds with aryl and alkenyl halides. The reactivity profile of copper catalysts is complementary to that of palladium catalysts in many cases. Copper catalysts are highly effective with less nucleophilic nitrogen nucleophiles, such as amides and azoles, whereas palladium catalysts are more effective with more nucleophilic amine nucleophiles. Copper is an attractive alternative to palladium due to its significantly lower cost. In addition, high activity palladium catalysts require expensive and often air-sensitive ligands, whereas the modern copper systems use relatively stable and inexpensive diamine or amino acid ligands. Copper-catalyzed C?N coupling reactions are tolerant of a wide range of functional groups and have been applied to the synthesis of a variety of complex natural products. Significant work has also been done to understand the mechanism of these reactions. Current mechanistic understanding of these methodologies is covered in this monograph. Note de contenu : " Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles". Cote : B-E094 Num_Inv : 3558 Localisation : LCC (SdS)

Exemplaires(1)

Code-barres	Cote	Support	Localisation	Section	Disponibilité
3558	B-E094	Texte imprimé	Bibliothèque	Livre	Disponible