scholarly journals Manganese‐Catalyzed Cross‐Coupling Processes

2021 ◽  
pp. 257-292
Author(s):  
Xiaoping Liu ◽  
Florian Jaroschik ◽  
Marc Taillefer
Keyword(s):  
Cross Coupling ◽  
Coupling Processes

Recent Developments in C–C Bond Formation Using Catalytic Reductive Coupling Strategies

Synthesis ◽  
2020 ◽  
Vol 52 (18) ◽  
pp. 2623-2638
Author(s):  
Joshua D. Sieber ◽  
Toolika Agrawal
Keyword(s):  
Bond Formation ◽  
Cross Coupling ◽  
Short Review ◽  
Reductive Coupling ◽  
Recent Developments ◽  
Molecular Complexity ◽  
Metal Catalyzed ◽  
Coupling Processes ◽  
Coupling Strategies

Metal-catalyzed reductive coupling processes have emerged as a powerful methodology for the introduction of molecular complexity from simple starting materials. These methods allow for an orthogonal approach to that of redox-neutral strategies for the formation of C–C bonds by enabling cross-coupling of starting materials not applicable to redox-neutral chemistry. This short review summarizes the most recent developments in the area of metal-catalyzed reductive coupling utilizing catalyst turnover by a stoichiometric reductant that becomes incorporated in the final product.1 Introduction2 Ni Catalysis3 Cu Catalysis4 Ru, Rh, and Ir Catalysis4.1 Alkenes4.2 1,3-Dienes4.3 Allenes4.4 Alkynes4.5 Enynes5 Fe, Co, and Mn Catalysis6 Conclusion and Outlook

Divergent synthesis of arylated pyridin-2(1H)-one derivatives via metal-catalysed cross-coupling processes

Tetrahedron ◽  
2010 ◽  
Vol 66 (32) ◽  
pp. 6138-6149 ◽  
Author(s):  
Jamie S. Siddle ◽  
Andrei S. Batsanov ◽  
Stuart T. Caldwell ◽  
Graeme Cooke ◽  
Martin R. Bryce
Keyword(s):  
Cross Coupling ◽  
Coupling Processes

Facile Access to 3,5-Dihalogenated Pyrazoles by Sydnone Cycloaddition and their Versatile Functionalization by Pd-Catalyzed Cross-Coupling Processes

2011 ◽  
Vol 2011 (20-21) ◽  
pp. 3837-3848 ◽  
Author(s):  
Thierry Delaunay ◽  
Mazen Es-Sayed ◽  
Jean-Pierre Vors ◽  
Nuno Monteiro ◽  
Geneviève Balme
Keyword(s):  
Cross Coupling ◽  
Coupling Processes
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