Issue 10, 2004

Enantioselective halogenation reactions

Abstract

Stereoselective halogenation reactions, in particular fluorinations, are not everyday's chemistry despite the fundamental and still increasing significance of fluorinated molecules, e.g., for the life science industry. The selective fluorination of a bioactive compound can be generally beneficial in terms of a possible increased intrinsic activity, enhanced chemical and metabolic stability, and improved pharmacokinetics. It is clear that more efficient and selective methodologies for the introduction of fluorine into organic molecules are still needed. We review in this article latest progresses in the area of enantioselective fluorinations, with particular emphasis on new catalytic reactions and extend our discussion to similar reactions involving the other halogens.

Graphical abstract: Enantioselective halogenation reactions

Article information

Article type
Feature Article
Submitted
06 Jan 2004
Accepted
10 Feb 2004
First published
08 Mar 2004

Chem. Commun., 2004, 1147-1155

Enantioselective halogenation reactions

H. Ibrahim and A. Togni, Chem. Commun., 2004, 1147 DOI: 10.1039/B317004G

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