Synthesis of α-Ethylidene β-lactones via lactonization/1,3-H-transposition of α-vinyl-β-hydroxy acids.

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Authors: Barnabas Otoo, Meklit Worku, Nick Griffin
Cited by: 0

Abstract

Since their discovery, β-lactones have garnered significant interest due to their unique chemistry and bioactivity. Our ongoing synthesis and evaluation of β-lactones for biological activity have revealed that DIC lactonization of α-vinyl and α-ethynyl β-EWG- β-hydroxy acids results in 1,3-H transposition, leading to the formation of α-alkylidene and α-allene lactones, respectively. The straightforward synthesis of these compounds will enable us to explore their utility for further chemical transformations.

Fields of Study & Subjects

Synthesis of β-Lactam Compounds Organic Chemistry Synthesis Methods Cyclopropane Reaction Mechanisms

Publication details

Journal / source
ChemRxiv
Publication date
6 February 2026
Document type
Preprint