TY - JOUR
T1 - Probability of spontaneously resolvable conglomerates for racemic acid/racemic amine salts predicted on the basis of the results of diastereomeric resolutions
AU - Kinbara, Kazushi
AU - Tagawa, Yoshiyuki
AU - Saigo, Kazuhiko
N1 - Funding Information:
This work was supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan.
PY - 2001/11/26
Y1 - 2001/11/26
N2 - The salts of racemic acids with racemic amines, of which the enantiopure component is a good resolving agent for the corresponding counterpart in diastereomeric resolution, have an extremely high tendency to be conglomerates: the results of diastereomeric resolutions are highly informative for the prediction of conglomerates, which can be enantioseparated by preferential crystallization developed independently from diastereomeric resolution over one and a half centuries.
AB - The salts of racemic acids with racemic amines, of which the enantiopure component is a good resolving agent for the corresponding counterpart in diastereomeric resolution, have an extremely high tendency to be conglomerates: the results of diastereomeric resolutions are highly informative for the prediction of conglomerates, which can be enantioseparated by preferential crystallization developed independently from diastereomeric resolution over one and a half centuries.
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U2 - 10.1016/S0957-4166(01)00527-4
DO - 10.1016/S0957-4166(01)00527-4
M3 - Article
AN - SCOPUS:0035956405
SN - 0957-4166
VL - 12
SP - 2927
EP - 2930
JO - Tetrahedron Asymmetry
JF - Tetrahedron Asymmetry
IS - 21
ER -