Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot process in aqueous medium at room temperature

2012 ◽  
Vol 84 ◽  
pp. 89-93 ◽  
Author(s):  
Sonja Borchert ◽  
Edyta Burda ◽  
Jürgen Schatz ◽  
Werner Hummel ◽  
Harald Gröger
Keyword(s):  
Aqueous Medium ◽  
Palladium Catalyst ◽  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Water Soluble ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Enzymatic Reduction

scholarly journals Room-temperature borylation and one-pot two-step borylation/Suzuki–Miyaura cross-coupling reaction of aryl chlorides

RSC Advances ◽  
2018 ◽  
Vol 8 (25) ◽  
pp. 13643-13648 ◽  
Author(s):  
Hong Ji ◽  
Li-Yang Wu ◽  
Jiang-Hong Cai ◽  
Guo-Rong Li ◽  
Na-Na Gan ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Aryl Chlorides ◽  
Highly Efficient ◽  
Cross Coupling Reaction

A highly efficient room-temperature strategy for borylation and one-pot two-step borylation/Suzuki–Miyaura cross-coupling reaction of aryl chlorides have been developed.

Umpolung Coupling of Pyridine-2-carboxaldehydes and Propargylic Carbonates via N-Heterocyclic Carbene/Palladium Synergetic Catalysis

2021 ◽  
Author(s):  
Weiyang Bi ◽  
Yunhui Yang ◽  
Song Ye ◽  
Congyang Wang
Keyword(s):  
Palladium Catalyst ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Cooperative Catalysis ◽  
Cross Coupling Reaction ◽  
First Time

The umpolung cross-coupling reaction of pyridine-2-carboxaldehydes and propargylic carbonates has been developed for the first time through N-heterocyclic carbene/palladium cooperative catalysis with the judicious selections of the palladium catalyst, ligand...

Synthesis of Shape-Persistent Macrocycles by a One-Pot Suzuki-Miyaura Cross-Coupling Reaction

2010 ◽  
Vol 17 (2) ◽  
pp. 440-444 ◽  
Author(s):  
Weiguo Huang ◽  
Ming Wang ◽  
Chun Du ◽  
Yulan Chen ◽  
Ruiping Qin ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Cross Coupling Reaction

Room-Temperature, Water-Promoted, Radical-Coupling Reactions of Phenols with tert-Butyl Nitrite

Synlett ◽  
2017 ◽  
Vol 28 (16) ◽  
pp. 2153-2156 ◽  
Author(s):  
Wen-Ting Wei ◽  
Hongze Liang ◽  
Wen-Ming Zhu ◽  
Weida Liang ◽  
Yi Wu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Phenol Derivative ◽  
Tert Butyl ◽  
Radical Coupling ◽  
Air Atmosphere ◽  
Cross Coupling Reaction ◽  
Temperature Water

A radical–radical cross-coupling reaction of phenols with tert-butyl nitrite has been developed with the use of water as an additive. This method allows the construction of C–N bonds under an air atmosphere at room temperature, providing the ortho-nitrated phenol derivative in moderate to good yields.

scholarly journals Factorial design evaluation of the Suzuki cross-coupling reaction using a magnetically recoverable palladium catalyst

2017 ◽  
Vol 58 (10) ◽  
pp. 903-908 ◽  
Author(s):  
Raíza R.G. Guerra ◽  
Felipe C.P. Martins ◽  
Carolina G.S. Lima ◽  
Ricardo H. Gonçalves ◽  
Edson R. Leite ◽  
...  
Keyword(s):  
Factorial Design ◽  
Palladium Catalyst ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Design Evaluation ◽  
Cross Coupling Reaction
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