Evaluation of Lewis Acidity of “Naked” Lithium Ion through Diels-Alder Reaction Catalyzed by Lithium TFPB in Nonpolar Organic Solvents

2000 ◽  
Vol 29 (1) ◽  
pp. 62-63 ◽  
Author(s):  
Kanji Fujiki ◽  
Shin-ya Ikeda ◽  
Hiroshi Kobayashi ◽  
Akira Mori ◽  
Akihisa Nagira ◽  
...  
ChemInform ◽  
2010 ◽  
Vol 31 (21) ◽  
pp. no-no
Author(s):  
Kanji Fujiki ◽  
Shin-ya Ikeda ◽  
Hiroshi Kobayashi ◽  
Akira Mori ◽  
Akihisa Nagira ◽  
...  

2017 ◽  
Vol 7 (5) ◽  
pp. 1045-1049 ◽  
Author(s):  
K. Matuszek ◽  
S. Coffie ◽  
A. Chrobok ◽  
M. Swadźba-Kwaśny

Ionic liquids with Lewis superacidic borenium cations were used as catalysts in solvent-less Diels–Alder cycloaddition. The extremely high catalytic activity correlated with the Lewis acidity, expressed as the Gutmann acceptor number.


Synlett ◽  
1999 ◽  
Vol 1999 (7) ◽  
pp. 1160-1162 ◽  
Author(s):  
Jun Mihara ◽  
Tetsuya Hamada ◽  
Tsuyoshi Takeda ◽  
Ryo Irie ◽  
Tsutomu Katsuki

ChemInform ◽  
2010 ◽  
Vol 30 (42) ◽  
pp. no-no
Author(s):  
Jun Mihara ◽  
Tetsuya Hamada ◽  
Tsuyoshi Takeda ◽  
Ryo Irie ◽  
Tsutomu Katsuki

2018 ◽  
Vol 50 (5) ◽  
pp. 319-324 ◽  
Author(s):  
Igor A. Sedov ◽  
Dmitry A. Kornilov ◽  
Vladimir D. Kiselev

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