ArticleJACS Au2021
Chiral Hypervalent Iodine Catalysis Enables an Unusual Regiodivergent Intermolecular Olefin Aminooxygenation.
Article in JACS Au, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
11 citing papers in PubMed.
- Bromonium-catalyzed 1,2-diamination of various conjugated alkenes.Chemical science · 2026Article
- Investigation of olefins as a cocatalyst for halonium catalysis.Chemical communications (Cambridge, England) · 2026Article
- Strategies for AccessingMolecules (Basel, Switzerland) · 2024Review
- Hypervalent iodine-catalyzed amide and alkene coupling enabled by lithium salt activation.Beilstein journal of organic chemistry · 2024Article
- Chemoselective cycloisomerization of O-alkenylbenzamides via concomitant 1,2-aryl migration/elimination mediated by hypervalent iodine reagents.Communications chemistry · 2023Article
- Tunable [3+2] and [4+2] annulations for pyrrolidine and piperidine synthesis.Chemical communications (Cambridge, England) · 2023Article
- A Facile Synthesis of 2-Oxazolines via Dehydrative Cyclization Promoted by Triflic Acid.Molecules (Basel, Switzerland) · 2022Article
- Regiodivergent Electrophotocatalytic Aminooxygenation of Aryl Olefins.Journal of the American Chemical Society · 2022Article
- Bifunctional sulfilimines enable synthesis of multiple N-heterocycles from alkenes.Nature chemistry · 2022Article
- Catalytic Synthesis of 5-Fluoro-2-oxazolines: Using BFACS omega · 2022Article
- Lewis Acid-Catalyzed Halonium Generation for Morpholine Synthesis and Claisen Rearrangement.The Journal of organic chemistry · 2022Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
A novel iodide-catalyzed intermolecular aminooxygenation strategy is described here. Amide is used as the O- and N- source to probe for regiocontrol strategies. Notably, simple additives can be selectively introduced to achieve regiodivergent oxyamination processes for electronically activated alkenes while being regio-complementary for unactivated alkenes. Our preliminary data demonstrates that this regiocontrol strategy based on nucleophile can also be applied in asymmetric processes using chiral hypervalent iodine catalysis.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.