@article{oai:nagasaki-u.repo.nii.ac.jp:00013371,
 author = {Onomura, Osamu and Ng’aNg’a, Wanyoike  George and Matsumura, Yoshihiro and Kuriyama, Masami},
 issue = {2},
 journal = {HETEROCYCLES},
 month = {Mar},
 note = {Memory of chirality in the electrochemical oxidation of thiazolidine-4-carboxylic acid derivatives was observed. The relatively larger size of sulphur atom than the oxygen atom for oxazolidine-4-carboxylic acid derivative may slightly improved the enantioselectivities of the oxidized products. The bulkier penicillamine derivative 1c furnished 2c with much better enantioselectivity (91% ee) than that of the cysteine derivative 2b (85% ee). The presence of two extra dimethyl groups, for the penicillamine derivative improved the enantioselectivities of the thiazolidine derivatives from 85% ee to 91 % ee., HETEROCYCLES, 80(2), pp.1177-1185; 2010},
 pages = {1177--1185},
 title = {Memory of Chirality in the Electrochemical Oxidation of Thiazolidine-4-carboxylic Acid Derivatives},
 volume = {80},
 year = {2010}
}