Regioselective synthesis of trifluoromethyl group substituted allylic amines via palladium-catalyzed allylic amination

2008 ◽  
Vol 49 (15) ◽  
pp. 2450-2453 ◽  
Author(s):  
Motoi Kawatsura ◽  
Takuya Hirakawa ◽  
Tomoko Tanaka ◽  
Daiji Ikeda ◽  
Shuichi Hayase ◽  
...  
Synlett ◽  
2010 ◽  
Vol 2010 (19) ◽  
pp. 2887-2890 ◽  
Author(s):  
Motoi Kawatsura ◽  
Toshiyuki Itoh ◽  
Takuya Hirakawa ◽  
Kazunori Ikeda ◽  
Hiroshi Ogasa

ChemInform ◽  
2012 ◽  
Vol 43 (12) ◽  
pp. no-no
Author(s):  
Takuya Hirakawa ◽  
Kazunori Ikeda ◽  
Daiji Ikeda ◽  
Tomoko Tanaka ◽  
Hiroshi Ogasa ◽  
...  

Tetrahedron ◽  
2011 ◽  
Vol 67 (43) ◽  
pp. 8238-8247 ◽  
Author(s):  
Takuya Hirakawa ◽  
Kazunori Ikeda ◽  
Daiji Ikeda ◽  
Tomoko Tanaka ◽  
Hiroshi Ogasa ◽  
...  

2017 ◽  
Vol 53 (37) ◽  
pp. 5151-5154 ◽  
Author(s):  
Jiangyan Jing ◽  
Xiaohong Huo ◽  
Jiefeng Shen ◽  
Jingke Fu ◽  
Qinghua Meng ◽  
...  

Allylic alcohols and allylic amines were directly utilized in a Pd-catalyzed hydrogen-bond-activated allylic amination under mild reaction conditions in the absence of any additives. The catalytic system is compatible with a variety of functional groups and can be used to prepare a wide range of linear allylic amines in good to excellent yields.


Tetrahedron ◽  
2017 ◽  
Vol 73 (19) ◽  
pp. 2766-2773 ◽  
Author(s):  
Alla Siva Reddy ◽  
A. Leela Siva Kumari ◽  
K.C. Kumara Swamy

Synthesis ◽  
2018 ◽  
Vol 51 (06) ◽  
pp. 1342-1352 ◽  
Author(s):  
Javier Izquierdo ◽  
Atul Jain ◽  
Sarki Abdulkadir ◽  
Gary Schiltz

The chromenone core is an ubiquitous group in biologically active natural products and has been extensively used in organic synthesis. Fluorine-derived compounds, including those with a trifluoromethyl group (CF3), have shown enhanced biological activities in numerous pharmaceuticals compared with their non-fluorinated analogues. 2-Trifluoromethylchromenones can be readily functionalized at the 8- and 7-positions, providing chromenones cores of high structural complexity, which are excellent precursors for numerous trifluoromethyl heterocycles.


2015 ◽  
Vol 137 (26) ◽  
pp. 8556-8563 ◽  
Author(s):  
Jie Liu ◽  
Qiang Liu ◽  
Robert Franke ◽  
Ralf Jackstell ◽  
Matthias Beller

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