Asymmetric induction in the reduction of optically active N-alkylidenesulphinamides by metal hydrides. A new, efficient enantioselective route to chiral amines

Author(s):  
Rita Annunziata ◽  
Mauro Cinquini ◽  
Franco Cozzi
1976 ◽  
Vol 7 (35) ◽  
pp. no-no
Author(s):  
R. HELDER ◽  
J. C. HUMMELEN ◽  
R. W. P. M. LAANE ◽  
J. S. WIERING ◽  
H. WYNBERG

2013 ◽  
Vol 3 (2) ◽  
pp. 119-126 ◽  
Author(s):  
Seongbum Kang ◽  
Inhwan Cha ◽  
Jeon Geon Han ◽  
Changsik Song

1998 ◽  
Vol 14 (1) ◽  
pp. 175-182 ◽  
Author(s):  
Koichiro NAEMURA ◽  
Kazuhisa MATSUNAGA ◽  
Junichi FUJI ◽  
Kazuko OGASAHARA ◽  
Yasushi NISHIKAWA ◽  
...  

1987 ◽  
Vol 65 (1) ◽  
pp. 195-199 ◽  
Author(s):  
Stephen Hanessian ◽  
Benoit Vanasse

A synthetic strategy towards tricholomic acid and acivicin has been established using the aldol condensation of N-pyruvilideneglycinatoaquocopper(II) and an optically active aldehyde derived from S-malic acid as the key bond-forming reaction. Although a viable strategy was developed, no asymmetric induction was observed.


Author(s):  
Jan H. Dopper ◽  
Ben Greijdanus ◽  
Dré Oudman ◽  
Hans Wynberg

Sign in / Sign up

Export Citation Format

Share Document