European Journal of Medicinal Chemistry p. 881 - 888 (1997)
Update date:2022-08-03
Topics:
Philippo
Fett
Bovy
Barras
Angel
Georges
Ochsenbein
Both enantiomers of 2-(dimethylamino)-1-[3- methoxy-2-(1-methylethoxy)phenyl]ethanol were synthetized by a stereoselective route and evaluated in vitro for their uroselectivity in comparison with other α1-adrenoceptor agonists. The most potent enantiomer was structurally characterized by X-ray crystallographic analysis.
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Doi:10.1007/BF00807103
(1997)Doi:10.1016/S0040-4020(97)00896-X
(1997)Doi:10.1016/S0957-4166(97)00381-9
(1997)Doi:10.1016/S0960-894X(98)00353-9
(1998)Doi:10.1021/acs.orglett.7b00784
(2017)Doi:10.1016/S0960-894X(97)00449-6
(1997)
