90104-03-3Relevant articles and documents
REACTIONS OF SCHIFF BASE ANIONS WITH ELECTROPHILES: ROLE OF THE INITIAL STEREOCHEMISTRY
El Achqar, Abdelrhani,Roumestant, Marie-Louise,Viallefont, Philippe
, p. 2441 - 2444 (2007/10/02)
It is shown that the reactivity towards electrophiles of diastereomeric Schiff bases of *R and *S valine, leucine, phenylalanine and norvaline methyl esters with (1S,2S,5S) or (1R,2R,5R) 2-hydroxy 3-pinanone, is highly dependent on the stereochemistry of the starting product.