Issue 15, 2014

Co(iii)(salen)-catalyzed phenolic kinetic resolution of two stereocentered benzyloxy and azido epoxides: its application in the synthesis of ICI-118,551, an anti-hypertensive agent

Abstract

The salen Co(III)-catalyzed phenolic kinetic resolution of racemic anti- or syn-azido and benzyloxy epoxides provides a practical route to a range of enantioenriched anti- or syn-1-aryloxy-3-azido or benzyloxy-2-alcohols in excellent yields and ees. The synthetic potential of this protocol is illustrated with an enantioselective synthesis of ICI-118,551, a β-blocker, in a highly optically pure form (99% ee).

Graphical abstract: Co(iii)(salen)-catalyzed phenolic kinetic resolution of two stereocentered benzyloxy and azido epoxides: its application in the synthesis of ICI-118,551, an anti-hypertensive agent

Supplementary files

Article information

Article type
Communication
Submitted
13 Dec 2013
Accepted
14 Feb 2014
First published
18 Feb 2014

Org. Biomol. Chem., 2014,12, 2349-2355

Co(III)(salen)-catalyzed phenolic kinetic resolution of two stereocentered benzyloxy and azido epoxides: its application in the synthesis of ICI-118,551, an anti-hypertensive agent

P. U. Karabal, D. A. Kamble and A. Sudalai, Org. Biomol. Chem., 2014, 12, 2349 DOI: 10.1039/C3OB42501K

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