Palladium(II)-assisted dialkylation and alkylation/acylation of optically active ene carbamates via trialkylorganostannane cross-coupling and carbonylative coupling processes

1991 ◽  
Vol 56 (19) ◽  
pp. 5666-5671 ◽  
Author(s):  
John J. Masters ◽  
Louis S. Hegedus ◽  
Joaquin Tamariz
Heterocycles ◽  
1992 ◽  
Vol 33 (2) ◽  
pp. 831 ◽  
Author(s):  
Seiichi Takano ◽  
Masashi Akiyama ◽  
Takumichi Sugihara ◽  
Kunio Ogasawara

Synthesis ◽  
2020 ◽  
Vol 52 (18) ◽  
pp. 2623-2638
Author(s):  
Joshua D. Sieber ◽  
Toolika Agrawal

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


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

ChemInform ◽  
2010 ◽  
Vol 23 (24) ◽  
pp. no-no
Author(s):  
R. ANNUNZIATA ◽  
M. BENAGLIA ◽  
M. CINQUINI ◽  
F. COZZI ◽  
P. GIARONI

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