Kinetic resolution of N-methyl-2-phenylpyrrolidine by cyclopalladation in the presence of an optically active base

1999 ◽  
Vol 35 (8) ◽  
pp. 1001-1011 ◽  
Author(s):  
V. V. Dunina ◽  
L. G. Kuz'mina ◽  
E. D. Razmyslova ◽  
V. P. Kislyi

ChemInform ◽  
2010 ◽  
Vol 31 (34) ◽  
pp. no-no
Author(s):  
V. V. Dunina ◽  
L. G. Kuz'mina ◽  
E. D. Razmyslova ◽  
V. P. Kislyi


1992 ◽  
Vol 65 (1) ◽  
pp. 111-120 ◽  
Author(s):  
Minoru Inagaki ◽  
Akihiko Hatanaka ◽  
Mitsuo Mimura ◽  
Jun Hiratake ◽  
Takaaki Nishioka ◽  
...  


Synthesis ◽  
2008 ◽  
Vol 2008 (14) ◽  
pp. 2283-2287 ◽  
Author(s):  
Klaus Ditrich


Molecules ◽  
2018 ◽  
Vol 23 (8) ◽  
pp. 2003 ◽  
Author(s):  
Takatsugu Murata ◽  
Tatsuya Kawanishi ◽  
Akihiro Sekiguchi ◽  
Ryo Ishikawa ◽  
Keisuke Ono ◽  
...  

Various optically active 2-hydroxyamide derivatives are produced based on the kinetic resolution of racemic 2-hydroxyamides with a diphenylacetyl component and (R)-benzotetramisole ((R)-BTM), a chiral acyl-transfer catalyst, via asymmetric esterification and acylation. It was revealed that a tertiary amide can be used with this novel protocol to achieve high selectivity (22 examples; s-value reaching over 250). The resulting chiral compounds could be transformed into other useful structures while maintaining their chirality.



Author(s):  
Valeria Merlo ◽  
Fiona J. Reece ◽  
Stanley M. Roberts ◽  
Mike Gregson ◽  
Richard Storer


2005 ◽  
Vol 16 (14) ◽  
pp. 2409-2416 ◽  
Author(s):  
Mei-Xiang Wang ◽  
Jun Liu ◽  
De-Xian Wang ◽  
Qi-Yu Zheng


Sign in / Sign up

Export Citation Format

Share Document