ChemInform Abstract: ASYMMETRIC INDUCTION DURING CARBONYLATION OF AN OPTICALLY ACTIVE ORGANOPALLADIUM. A NOVEL AND VERSATILE ROUTE TO ENANTIOMERIC GLYCERIDES

1985 ◽  
Vol 16 (39) ◽  
Author(s):  
L. L. TROITSKAYA ◽  
V. I. SOKOLOV
1976 ◽  
Vol 7 (35) ◽  
pp. no-no
Author(s):  
R. HELDER ◽  
J. C. HUMMELEN ◽  
R. W. P. M. LAANE ◽  
J. S. WIERING ◽  
H. WYNBERG

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

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