scholarly journals Carbonylative Cross-Coupling ofortho-Disubstituted Aryl Iodides. Convenient Synthesis of Sterically Hindered Aryl Ketones

2008 ◽  
Vol 10 (22) ◽  
pp. 5301-5304 ◽  
Author(s):  
B. Michael O’Keefe ◽  
Nicholas Simmons ◽  
Stephen F. Martin
Tetrahedron ◽  
2011 ◽  
Vol 67 (24) ◽  
pp. 4344-4351 ◽  
Author(s):  
B. Michael O’Keefe ◽  
Nicholas Simmons ◽  
Stephen F. Martin

Author(s):  
Pan Xie ◽  
Cheng Xue ◽  
Cancan Wang ◽  
Dongdong Du ◽  
Sanshan Shi

A CF3SO2Na/Pd(OAc)2 co-catalyzed strategy is developed to produce aryl ketones via visible-light-induced decarboxylative cross-coupling of α-oxocarboxylic acids and aryl boronic acids. This process was perfomed under air at room temperature,...


2021 ◽  
Author(s):  
Travis DeLano ◽  
Sara Dibrell ◽  
Caitlin R. Lacker ◽  
Adam Pancoast ◽  
Kelsey Poremba ◽  
...  

An asymmetric reductive cross-coupling of α-chloroesters and (hetero)aryl iodides is reported. This nickel-catalyzed reaction proceeds with a chiral BiOX ligand under mild conditions, affording α-arylesters in good yields and enantioselectivities....


2021 ◽  
Author(s):  
Yuliang Liu ◽  
Haoyu Li ◽  
Shunsuke Chiba
Keyword(s):  

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