Shinobu Takizawa & Mohamed S. H. Salem 
Atropisomerism in Asymmetric Organic Synthesis [PDF ebook] 
Challenges and Applications

Apoio

Unique overview of the recent synthetic methodologies of the atropisomeric molecules and their numerous practical applications

Atropisomerism in Asymmetric Organic Synthesis: Challenges and Applications presents new methodologies, strategies, unique catalysts, and solutions to challenges in the area of oxidative heterocoupling. After a general introduction for the concept of atropisomerism, this book focuses on the recent advances in the atroposelective synthesis of axially chiral compounds and how these advances had a significant impact on several applications in asymmetric catalysis and the synthesis of natural products.

The book covers the recent examples of metal-catalyzed (Cu, Fe, Ru, V, etc) and organocatalyzed atroposelective syntheses of axially chiral compounds using diverse approaches, including cross-coupling reactions, ring-opening reactions, formation of new aromatic rings, and desymmetrization via functional group transformation. The impact of these efficient strategies on various applications in asymmetric catalysis, total synthesis of natural products, synthesis of polycyclic heteroaromatics (PHAs), and the drug industry is also addressed.

Edited by two highly qualified academics, Atropisomerism in Asymmetric Organic Synthesis explores sample topics including:


  • Iron- and ruthenium-catalyzed atroposelective synthesis of axially chiral compounds and the catalytic applications of multinuclear zinc complexes with axially chirality

  • Vanadium-catalyzed atroposelective coupling of arenols and application in the synthesis of polycyclic heteroaromatics PHAs

  • Mechanisms of atroposelective Suzuki-Miyaura coupling towards axially chiral biaryls and organocatalytic enantioselective formation of atropisomers

  • Synthesis of atropisomers via enantioselective ring-opening reactions and the impact of axially chiral ligands and catalysts derived from atropisomeric binaphthyl structures

  • Binaphthyl-based chiral DMAP derivatives in enantioselective transformations and catalytic atroposelective oxidative coupling in natural product synthesis


Enabling readers to comprehensively understand the development history, research status, and potential of atropisomeric synthesis, Atropisomerism in Asymmetric Organic Synthesis is an essential, up-to-date reference for researchers and scientists in the field.

€124.99
Métodos de Pagamento

Tabela de Conteúdo

1. Introduction (General Methods for the Construction of Atropisomers

2. Copper-Catalyzed Atroposelective Homo/ and Heterocoupling of Axially Chiral Compounds

3. (Fe, Ru)-Catalyzed Atroposelective Synthesis of Axially Chiral Compounds

4. Vanadium-Catalyzed Atroposelective Coupling of Arenols and Their Application in the Synthesis of PHAs

5. (Cu, Cr, V)-Catalyzed Atroposelective Coupling of Arenols

6. Iron-Catalyzed Atroposelective Synthesis of Axially Chiral Compounds

7. Bio/Metal Hybrid Systems for the Atroposelective Synthesis

8. Atroposelective Synthesis and Its Applications in The Field of Asymmetric Catalysis

9. Atroposelective Synthesis of Complex, Biologically Active Natural Products

10. Application of Atropisomerism in Total Synthesis of Naphthylisoquinoline (NIQ) Alkaloids

11. Atropoisomerism in the Field of Asymmetric Organocatalysis

Sobre o autor

Shinobu Takizawa, Ph D, is Professor at SANKEN, Osaka University, Japan. His current research focuses on developing environmentally friendly organic synthetic processes.
Mohamed S. H. Salem, Ph D, is Assistant Professor at SANKEN, Osaka University, Japan. His current research focuses on developing green synthetic approaches for the bottom-up synthesis of functionalized small organic molecules with various material-based applications.
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Língua Inglês ● Formato PDF ● Páginas 355 ● ISBN 9783527844234 ● Tamanho do arquivo 14.0 MB ● Editor Shinobu Takizawa & Mohamed S. H. Salem ● Editora Wiley-VCH ● País DE ● Publicado 2024 ● Edição 1 ● Carregável 24 meses ● Moeda EUR ● ID 9973750 ● Proteção contra cópia Adobe DRM
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