Oxidative deamination of sec-alkyl primary amines with 3,5-di-tert-butyl-1,2-benzoquinone; a second look

1988 ◽  
Vol 53 (26) ◽  
pp. 5994-5998 ◽  
Author(s):  
Robert F. X. Klein ◽  
Lisa M. Bargas ◽  
Vaclav Horak
Synlett ◽  
1990 ◽  
Vol 1990 (10) ◽  
pp. 621-623 ◽  
Author(s):  
Martyn J. Earle ◽  
Robin A. Fairhurst ◽  
Harry Heaney ◽  
George Papageorgiou

1999 ◽  
Vol 82 (9) ◽  
pp. 1502-1508 ◽  
Author(s):  
Bruno Danieli ◽  
Giordano Lesma ◽  
Daniele Passarella ◽  
Davide Prosperi ◽  
Alessandra Silvani ◽  
...  

2002 ◽  
Vol 55 (12) ◽  
pp. 789 ◽  
Author(s):  
Rohan A. Davis ◽  
Anthony R. Carroll ◽  
Ronald J. Quinn

The synthesis of the novel biaryl compound, 4-(2-thienyl)-1H-pyrrole-2-carbaldehyde (1), by Suzuki–Miyaura coupling conditions is reported. Compound (1) was subsequently used as a combinatorial template in the parallel solution-phase synthesis of an amine and imine compound library. The amine library was produced using reductive amination conditions, and purification was achieved by a liquid–liquid partition followed by silica chromatography to afford ten amine analogues. The imine library consisted of five compounds, which were synthesized using volatile primary amines that allowed purification by evaporation. The synthesis of the novel and related biaryl carbaldehyde, tert-butyl-2-(5-formyl-1H-pyrrol-3-yl)-1H-pyrrole-1-carboxylate (2) is also reported.


2001 ◽  
Vol 30 (7) ◽  
pp. 712-713 ◽  
Author(s):  
Jun-ichi Matsuo ◽  
Asahi Kawana ◽  
Yoshio Fukuda ◽  
Teruaki Mukaiyama

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