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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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Detalles Bibliográficos
Autores principales:	Bovonsombat, Pakorn, Sophanpanichkul, Punyanuch, Losuwanakul, Satreerat
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Royal Society of Chemistry 2022
Materias:	Chemistry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373005/ https://www.ncbi.nlm.nih.gov/pubmed/36105984 http://dx.doi.org/10.1039/d2ra03540e

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