Regioselective Synthesis of Nitrones by Decarboxylative Oxidation ofN-Alkyl-α-amino Acids and Application to the Synthesis of 1-Azabicyclic Alkaloids

1999 ◽  
Vol 72 (12) ◽  
pp. 2737-2754 ◽  
Author(s):  
Hiroaki Ohtake ◽  
Yasushi Imada ◽  
Shun-Ichi Murahashi
2019 ◽  
Vol 2019 (8) ◽  
pp. 1820-1824 ◽  
Author(s):  
Rafat Ali ◽  
Mohd. Zisan Ahamad ◽  
Shalini Singh ◽  
Wahajul Haq

2004 ◽  
Vol 6 (13) ◽  
pp. 2273-2276 ◽  
Author(s):  
Jin Hyo Kim ◽  
Marcus J. C. Long ◽  
Jun Young Kim ◽  
Ki Hun Park

1988 ◽  
Vol 29 (42) ◽  
pp. 5365-5368 ◽  
Author(s):  
Christophe Ruppin ◽  
Pierre H. Dixneuf ◽  
Serge Lecolier

ChemInform ◽  
2004 ◽  
Vol 35 (41) ◽  
Author(s):  
Jin Hyo Kim ◽  
Marcus J. C. Long ◽  
Jun Young Kim ◽  
Ki Hun Park

2014 ◽  
Vol 10 ◽  
pp. 117-126 ◽  
Author(s):  
Tatyana L Pavlovskaya ◽  
Fedor G Yaremenko ◽  
Victoria V Lipson ◽  
Svetlana V Shishkina ◽  
Oleg V Shishkin ◽  
...  

The regioselective three-component condensation of azomethine ylides derived from isatins and α-amino acids with acrylamides or aroylacrylic acids as dipolarophiles has been realized through a one-pot 1,3-dipolar cycloaddition protocol. Decarboxylation of 2'-aroyl-2-oxo-1,1',2,2',5',6',7',7a'-octahydrospiro[indole-3,3'-pyrrolizine]-1'-carboxylic acids is accompanied by cyclative rearrangement with formation of dihydropyrrolizinyl indolones.


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