Selective Fluoromethyl Couplings of Alkynes via Nickel Catalysis**

Author(s):  
Huan Li ◽  
Fang Wang ◽  
Shengqing Zhu ◽  
Lingling Chu
Keyword(s):  
ChemInform ◽  
2010 ◽  
Vol 28 (10) ◽  
pp. no-no
Author(s):  
Y. GAI ◽  
M. JULIA ◽  
J.-N. VERPEAUX
Keyword(s):  

Synlett ◽  
2020 ◽  
Author(s):  
Shengqing Zhu ◽  
Lingling Chu ◽  
Xiaoliang Feng ◽  
Lei Guo

AbstractA formal ethylene alkylarylation reaction with aryl halides and alkyl oxalates enabled by synergistic photoredox/nickel catalysis is reported. This protocol takes advantage of borates as a traceless activation group, achieving the formal ethylene difunctionalized products via a catalytic three-component 1,2-alkylarylation of vinyl borate followed by a base-assisted deborylation process. The mild conditions allow for excellent functional groups compatibility and broad substrate scope.


Author(s):  
Wei-Ze Li ◽  
Zhong-Xia Wang
Keyword(s):  

α-Alkylation of methyldiarylphosphine oxides and dialkyl methylphosphonates with (hetero)arylmethyl alcohols was performed under nickel catalysis.


2019 ◽  
Vol 25 (35) ◽  
pp. 8371-8386 ◽  
Author(s):  
Irene Erdelmeier ◽  
Gerd Bülow ◽  
Chang‐Wan Woo ◽  
Jürgen Decker ◽  
Gerhard Raabe ◽  
...  

1981 ◽  
Vol 22 (36) ◽  
pp. 3463-3466 ◽  
Author(s):  
Barry M. Trost ◽  
Paul L. Ornstein
Keyword(s):  

2011 ◽  
Vol 50 (31) ◽  
pp. 7022-7026 ◽  
Author(s):  
Takehisa Maekawa ◽  
Hiromi Sekizawa ◽  
Kenichiro Itami
Keyword(s):  

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