4.7 Article

An efficient asymmetric synthesis of (S)-atenolol:: using hydrolytic kinetic resolution

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 13, Issue 3, Pages 627-630

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2004.10.057

Keywords

beta-blockers; atenolol; Jacobsen catalyst; enantiomers; isopropylamine

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Enantiomerically pure (S)-atenolol was prepared by using (R,R) salen Co(III) complex for the resolution of terminal epoxide. This process was carried out at room temperature in excellent enantio selectivity. The method can be applied for large-scale preparation of (S)-atenolol without any problem. (C) 2004 Elsevier Ltd. All rights reserved.

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