A New Synthesis of Primary Amines Usingtert-Butylamine as an Ammonia Equivalent: The Triflic Acid Catalysed Removal ofN-tert-Butyl Groups from Carbamates

Synlett ◽  
1990 ◽  
Vol 1990 (10) ◽  
pp. 621-623 ◽  
Author(s):  
Martyn J. Earle ◽  
Robin A. Fairhurst ◽  
Harry Heaney ◽  
George Papageorgiou
1986 ◽  
Vol 27 (34) ◽  
pp. 3957-3960 ◽  
Author(s):  
Franklin A. Davis ◽  
Mark A. Giangiordano ◽  
William E. Starner
Keyword(s):  

Synthesis ◽  
2020 ◽  
Vol 52 (14) ◽  
pp. 2031-2037
Author(s):  
Antonio Leyva-Pérez ◽  
María Tejeda-Serrano ◽  
Sergio Sanz-Navarro ◽  
Finn Blake

Zeolites are the most used catalysts worldwide in petrochemistry processes, with particular ability to stabilize carbocations. However, the use of zeolites in organic synthesis is still scarce. We show here that representative carboxonium-mediated organic reactions, such as the Nazarov cyclization and the tert-butylation of alcohols with tert-butyl acetate, typically performed with very strong acid catalysts in solution such as triflic acid, can be catalyzed by simple zeolites with high yield and selectivity. The aluminosilicate framework stabilizes the intermediate carboxonium species and overrides the need for superacid protons in solution.


1988 ◽  
Vol 53 (26) ◽  
pp. 5994-5998 ◽  
Author(s):  
Robert F. X. Klein ◽  
Lisa M. Bargas ◽  
Vaclav Horak

ChemInform ◽  
2010 ◽  
Vol 25 (10) ◽  
pp. no-no
Author(s):  
N. A. MUKMENEVA ◽  
O. A. CHERKASOVA ◽  
V. KH. KADYROVA
Keyword(s):  

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