Electrophilic halogenations of propargyl alcohols: paths to α-haloenones, β-haloenones and mixed β,β-dihaloenones
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DOI: 10.1039/d2ra03540e
Abstract: 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… read more here.
Keywords: propargyl alcohols; electrophilic halogenations; mixed dihaloenones; halogenations propargyl ... See more keywords