Electrophilic halogenations of propargyl alcohols: paths to α-haloenones, β-haloenones and mixed β,β-dihaloenones

The Meyer-Schuster rearrangement of propargyl alcohols or alkynols leading to α,β-unsaturated carbonyl compounds is well known. Yet, electrophilic halogenations of the same alkynols and their alkoxy, ester and halo derivatives are inconspicuous. This review on the halogenation reactions of propargyl...

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Bibliographic Details
Main Author: Bovonsombat P.
Other Authors: Mahidol University
Format: Review
Published: 2023
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/87503
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Institution: Mahidol University

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