A Mild and Efficient Method for Racemization of α-Amino Esters.

ChemInform ◽  
2004 ◽  
Vol 35 (17) ◽  
Author(s):  
Uma Ramachandran ◽  
Sudhanshu Kumar ◽  
H. P. S. Chawla
Synlett ◽  
2017 ◽  
Vol 28 (18) ◽  
pp. 2483-2488 ◽  
Author(s):  
Bo Jiang ◽  
Guigen Li ◽  
Shuo Qiao ◽  
Jianbin Wu ◽  
Junming Mo ◽  
...  

A series of new chiral N-phosphinyl β-enamino esters and amides were successfully prepared with excellent Z-stereoselectivity (Z/E > 99:1 in nearly all cases). Group-assisted purification chemistry proved to be an efficient method for the asymmetric reduction of the resulting β-enamino esters/amides to give enantiopure β-amino esters/amides. The asymmetric reduction can be controlled efficiently by using a combination of sodium cyanoborohydride and acetic acid.


ChemInform ◽  
2010 ◽  
Vol 42 (4) ◽  
pp. no-no
Author(s):  
Marco Pallavicini ◽  
Cristiano Bolchi ◽  
Laura Fumagalli ◽  
Oreste Piccolo ◽  
Ermanno Valoti

2014 ◽  
Vol 26 (4) ◽  
pp. 1171-1173 ◽  
Author(s):  
Yanmei Zhao ◽  
Zhouyu Wang ◽  
Zhenju Jiang ◽  
Hualin Feng ◽  
Li Liu ◽  
...  

2010 ◽  
Vol 51 (42) ◽  
pp. 5540-5542 ◽  
Author(s):  
Marco Pallavicini ◽  
Cristiano Bolchi ◽  
Laura Fumagalli ◽  
Oreste Piccolo ◽  
Ermanno Valoti

2003 ◽  
Vol 35 (6) ◽  
pp. 616-619 ◽  
Author(s):  
Uma Ramachandran ◽  
Sudhanshu Kumar ◽  
H. P. S. Chawla

2012 ◽  
Vol 8 ◽  
pp. 1564-1568 ◽  
Author(s):  
Zhanwei Xu ◽  
Xiaoqiang Yu ◽  
Xiujuan Feng ◽  
Ming Bao

An efficient method for the synthesis of arylglycine derivatives is described. The oxidative coupling reactions of naphthols and phenols with α-amino esters proceeded smoothly in the presence of meta-chloroperoxybenzoic acid as an oxidant under ambient conditions, to produce arylglycine derivatives in satisfactory yields.


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