
Journal of Medicinal Chemistry p. 870 - 875 (1985)
Update date:2022-08-05
Topics:
Ross
Wiley
Since the Z isomer of chlorprothixene is far more active than its E counterpart, it was of interest to develop a stereoselective synthesis for this class of compounds. Insertion of a benzenesulfonamido group at the peri position of a chlorprothixene precu
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(1985)Doi:10.1039/jr9620004039
(1962)Doi:10.1248/cpb.32.4662
(1984)Doi:10.1016/j.ica.2004.03.002
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