ArticleAngewandte Chemie (International ed. in English)2024
α-Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping.
Article in Angewandte Chemie (International ed. in English), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Photoinduced intramolecular S-α-C(spChemical science · 2026Article
- Carbonyl-to-sulfur swap enabled by sequential double carbon-carbon bond activation.Science (New York, N.Y.) · 2025Article
- Microfluidic Photocatalytic Ring Expansion of Sulfonium Salts for the Synthesis of Cyclic Sulfides.ACS catalysis · 2025Article
- α-Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping.Angewandte Chemie (International ed. in English) · 2024Article
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Authors and funding
7 authors.
Funding
Abstract
A general and straightforward procedure for the lithiation trapping of cyclic sulfides such as tetrahydrothiophene, tetrahydrothiopyran and a thiomorpholine is described. Trapping with a wide range of electrophiles is demonstrated, leading to more than 50 diverse α-substituted saturated sulfur heterocycles. The methodology provides access to a range of α-substituted cyclic sulfides that are not easily synthesised by the currently available methods.
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Registered trials
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