[Aboul-Enein HY, Bakr SA. Enantiomeric resolution of propranolol and analogs on two cellulose (Chiracel of and OC) and one amylose (Chiracel AD) chiral stationary phases. J Liq Chrom & Relat Techn. 1998;8:1137-1145.10.1080/10826079808006589]Search in Google Scholar
[Bevinakatti, HS, Banerji AA. Practical chemoenzymic synthesis of both enantiomers of propranolol. J Org Chem. 1991;56:5372-5375.10.1021/jo00018a032]Search in Google Scholar
[Bojarski J. Stereoselective chromatography of cardiovascular drugs: an update. J Biochem Biophys Methods. 2002;54:197-220.10.1016/S0165-022X(02)00143-4]Search in Google Scholar
[Bruchatá K, Čižmáriková R, Hroboňová K, Lehotay J, Kyselová Z. Synthesis and study of enantioseparation of some potencial β-blockers of aryloxyaminopropanol type by HPLC using macrocyclic antibiotics as chiral selector. Acta Fac Pharm Univ Comen. 2006;53:68-75.]Search in Google Scholar
[Crowter AF, Smith LH. Beta-adrenergic blocking agents II. Propranolol and related 3-amino-1-naphthoxy-2-propanols. J Med Chem. 1968;11:1009-1013.10.1021/jm00311a021]Search in Google Scholar
[Čižmáriková R, Hroboňová K, Lehotay J, Račanská E, Bruchatá K. Preparation, pharmacological activity and enantioseparation of [3-cyclopentyloxymethyl)-4-(2-hydroxy-3-isopropylaminopropoxy)phenyl]ethanone as potential β-blocker. Acta Fac Pharm Univ Comen. 2005;52:79-88.]Search in Google Scholar
[Čižmáriková R. β-Adrenergic receptor blockers-the group of chiral drugs: Different effect of individual enantiomers (in Slovak). Čes slov Farm. 2002;51:121-128.]Search in Google Scholar
[Eshghi H, Porkar YH. A facile synthesis of (S)-(-)propranolol. J Sci I R Iran. 2003;14:17-19.]Search in Google Scholar
[Fischer W. Anticonvulsant profile and mechanism of action of propranolol and its two enantiomers. Seizure. 2002;11:285-302.10.1053/seiz.2001.0644]Search in Google Scholar
[Florenz J, Pomor JL, Malpartida F. Beta-adrenergic blockade and antiarrhythmic activity of (-) and (+) propranolol. Rev Espan Fisiol. 1969;25:287-292.]Search in Google Scholar
[Lohman D, Lehmann D, Morgenstern E, Faust G. Synthese and antikonvulsive Wirkung von Propranolol Derivaten mit tertiärem Stickstoffatom. Pharmazie. 1990;45:401-403.]Search in Google Scholar
[Mathett MW, Branch SK, Jefferies TM. Polar organic chiral separation of propranolol and analogues using a β-cyclodextrin bonded stationary phase. Chirality. 1996;8:126-130.10.1002/(SICI)1520-636X(1996)8:1<126::AID-CHIR18>3.0.CO;2-P]Search in Google Scholar
[Ram N, Heilman RD, Greenslade FC. Antihypertensive activity of a propranolol analog (ORF 12, 592) in rodents. Arch. Int Pharmacodyn Ther. 1976;224:102-108.]Search in Google Scholar
[Schaus ES, Brandes BD, Larrow JF, Tokunaga M, Hansen KB, Gould AF, Furrow MF, Jacobsen EN. Highly selective hydrolytic kinetic resolution of terminal epoxides catalyzed by chiral (salen) Co III comlexes. Practical synthesis of enantioenriched terminal epoxides and 1,2-diols. J Am Chem Soc. 2002;124:1307-1315.10.1021/ja016737l]Search in Google Scholar
[Valentová J, Čižmåiková R, Bui TTT, Drake AF, Hull AJ. Enantiomeric resolution of novel aryloxyaminopropanol derivatives with β-adrenoceptor antagonist activity on a derivatised amylose chiral stationary. Chromatographia. 2003;11/12:733-740.]Search in Google Scholar