ArticleJournal of the American Chemical Society2021
Palladium-Catalyzed Annulations of Strained Cyclic Allenes.
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 14 papers.
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Who cites it
14 citing papers in PubMed.
- Tandem cyclohexen-3-yne and 1,2,3-cyclohexatriene reactions.Nature communications · 2026Article
- Identification of natural products and synthetic analogs which inhibit microsporidia spores and prevent infection.Journal of invertebrate pathology · 2026Article
- Geometric distortion as an enabling tool for organic synthesis.Nature synthesis · 2025Article
- Diels-Alder Cycloadditions of Oxacyclic Allenes and α-Pyrones.Organic letters · 2024Article
- Access to Complex Scaffolds Through [2 + 2] Cycloadditions of Strained Cyclic Allenes.Journal of the American Chemical Society · 2024Article
- Generation and reactivity of unsymmetrical strained heterocyclic allenes.Nature synthesis · 2024Article
- Cyclic Allene Approach to the Manzamine Alkaloid Keramaphidin B.Organic letters · 2023Article
- Catalyst-Controlled Annulations of Strained Cyclic Allenes with π-Allylpalladium Complexes.Journal of the American Chemical Society · 2023Article
- Total synthesis of lissodendoric acid A via stereospecific trapping of a strained cyclic allene.Science (New York, N.Y.) · 2023Article
- Merging Metals and Strained Intermediates.Chem catalysis · 2022Article
- π-Extension of heterocyclesChemical science · 2022Article
- Pd-Catalyzed Heteroannulation UsingJournal of the American Chemical Society · 2022Article
- Interception of 1,2-cyclohexadiene with TEMPO radical.Tetrahedron letters · 2021Article
- Review
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
We report Pd-catalyzed annulations of in situ generated strained cyclic allenes. This methodology employs aryl halides and cyclic allene precursors as the reaction partners in order to generate fused heterocyclic products. The annulation proceeds via the formation of two new bonds and an sp
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Registered trials
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