Providing comprehensive insight into the use of copper in
cross-coupling reactions, Copper-Mediated Cross-Coupling
Reactions provides a complete up-to-date collection of the
available reactions and catalytic systems for the formation of
carbon-heteroatom and carbon-carbon bonds. This essential reference
covers a broad scope of copper-mediated reactions, their
variations, key advances, improvements, and an array of academic
and industrial applications that have revolutionized the field of
organic synthesis. The text also discusses the mechanism of
these transformations, the use of copper as cost-efficient
alternative to palladium, as well as recently developed methods for
conducting copper-mediated reactions with supported catalysts.
Tabla de materias
Preface: Copper Catalysis from a Historical Perspective: A Legacy from the Past
Gwilherm Evano and Nicolas Blanchard
PART 1 FORMATION OF C-HETEROATOM BONDS
Chapter 1: Modern Ullmann-Goldberg Chemistry: Arylation of N-nucleophiles with Aryl Halides
Yongwen Jiang and Dawei Ma
Chapter 2: Ullmann Condensation Today: Arylation of Alcohols and Thiols with Aryl Halides
Anis Tlili and Marc Taillefer
Chapter 3: Copper-Catalyzed Formation of C-P Bonds with Aryl Halides
Carole Alayrac and Annie-Claude Gaumont
Chapter 4: Alternative and Emerging Reagents for the Arylation of Heteronucleophiles
Luc Neuville
Chapter 5: Beyond Ullmann-Goldberg Chemistry: Vinylation, Alkynylation and Allenylation of Heteronucleophiles
Kévin Jouvin and Gwilherm Evano
Chapter 6: Aromatic/Vinylic Finkelstein Reaction
Alicia Casitas and Xavi Ribas
Chapter 7: Insights into the Mechanism of Modern Ullmann-Goldberg Coupling Reactions
Alicia Casitas and Xavi Ribas
PART 2 FORMATION OF C-C BONDS
Chapter 8: Modern Copper-Catalyzed Hurtley Reaction: Efficient C-Arylation of CH-Acid Derivatives
Irina P Beletskaya and Alexey Yu Fedorov
Chapter 9: Copper-Catalyzed Cyanations of Aryl Halides and Related Compounds
Thomas Schareina and Matthias Beller
Chapter 10: Copper-Mediated Aryl-aryl Bond Formation Leading to Biaryls: A Century after the Ullmann Breakthrough
Yoshihiko Yamamoto
Chapter 11: Copper-Catalyzed Alkynylation, Alkenylation and Allylation Reactions of Aryl Derivatives
Ren-Jie Song and Jin-Heng Li
Chapter 12: Copper-Catalyzed Alkynylation and Alkenylation Reaction of Alkynyl Derivatives: New Access to Diynes and Enynes
Ruimao Hua
Chapter 13: Copper-Mediated Alkenylation Reaction of Alkenyl Derivatives: a Straightforward Elaboration of 1, 3-Dienes
Hao Li, Songbai Liu, and Lanny S Liebeskind
Chapter 14: Emerging Areas in Copper-Mediated Trifluoromethylations of Aryl Derivatives: Catalytic and Oxidative Cross-Coupling Processes
Kévin Jouvin, Céline Guissart, Cédric Theunissen and Gwilherm Evano
PART 3 APPLICATIONS OF COPPER-CATALYZED CROSS-COUPLING REACTIONS: HETEROCYCLES, NATURAL PRODUCTS, PROCESS AND SUSTAINABLE CHEMISTRY
Chapter 15: Copper-Mediated Cyclization Reactions: New Entries to Heterocycles
Daoshan Yang and Hua Fu
Chapter 16: Application of Copper-Mediated C-N Bond Formation in Complex Molecules Synthesis
Jihoon Lee and James S Panek
Chapter 17: Natural Products and C-O/C-S Bond Forming Reactions: Copper Showed the Way
Doron Pappo
Chapter 18: Copper-Catalyzed C-C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection
Morgan Donnard and Nicolas Blanchard
Chapter 19: Process Chemistry and Copper Catalysis
Klaus Kunz and Norbert Lui
Chapter 20: Reusable Catalysts for Copper-Mediated Cross-Coupling Reactions under Heterogeneous Conditions
Zhiyong Wang, Changfeng Wan and Ye Wang
Sobre el autor
GWILHERM EVANO is a Professor at the Université
Libre de Bruxelles and the Co-Director of the Laboratory of Organic
Chemistry. Prof. Evano’s research focuses on the development of
copper-mediated transformations, chemistry of ynamides and other
hetero-substituted alkynes, and total synthesis of natural
products.
NICOLAS BLANCHARD is Research Director at the French
National Center for Scientific Research at the University of
Strasbourg. Dr. Blanchard’s research interests focus on the
synthesis of biologically relevant compounds using metal-mediated
transformations.
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