ArticleJournal of the American Chemical Society2021
Rapid Assembly of Tetrasubstituted Furans via Pummerer-Type Rearrangement.
Article in Journal of the American Chemical Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 37 citations in OpenAlex.
- Sulfur-Directed Construction of Vinyl Cyclopropanes from 1,3-Dienes.Angewandte Chemie (International ed. in English) · 2026Article
- Thiophene Derivatives as Versatile Precursors for (Hetero)Arene and Natural Product Synthesis.Angewandte Chemie (International ed. in English) · 2026Review
- Metal-Free Catalytic Synthesis of Tetrasubstituted Furans fromMolecules (Basel, Switzerland) · 2025Article
- Catalytic [4+2]- and [4+4]-cycloaddition using furan-fused cyclobutanone as a privileged C4 synthon.Nature communications · 2024Article
- Mechanistic Insights into the Formation of 1-Alkylidene/Arylidene-1,2,4-triazolinium Salts: A Combined NMR/Density Functional Theory Approach.The Journal of organic chemistry · 2022Article
- Multicomponent formation route to a new class of oxygen-based 1,3-dipoles and the modular synthesis of furans.Chemical science · 2021Article
- Synthesis of Pyrroles via Consecutive 6π-Electrocyclization/Ring-Contraction of Sulfilimines.Journal of the American Chemical Society · 2021Article
Corrections and comments
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
Abstract
Despite the many methods available for the synthesis of furans, few methods remain that allow for the custom-made assembly of fully substituted furans. Here we report a powerful protocol to rapidly construct tetrasubstituted, orthogonally functionalized furans under mild reaction conditions. The developed method involves the regioselective ring-opening of readily available 2,5-dihydrothiophenes followed by an oxidative cyclization to provide the heterocycle. The selective oxidation at sulfur is promoted by
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Registered trials
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