ArticleOrganic letters2016
Pd-Catalyzed Suzuki-Miyaura and Hiyama-Denmark Couplings of Aryl Sulfamates.
Article in Organic letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Broad-Scope Amination of Aryl Sulfamates Catalyzed by a Palladium Phosphine Complex.ACS catalysis · 2023Article
- Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications.Molecules (Basel, Switzerland) · 2022Review
- Differences in the Performance of Allyl Based Palladium Precatalysts for Suzuki-Miyaura Reactions.Advanced synthesis & catalysis · 2020Article
- Palladium-Catalyzed Cross-Couplings by C-O Bond Activation.Catalysis science & technology · 2020Article
- Palladium Complexes Based on Ylide-Functionalized Phosphines (YPhos): Broadly Applicable High-Performance Precatalysts for the Amination of Aryl Halides at Room Temperature.Chemistry (Weinheim an der Bergstrasse, Germany) · 2020Article
- Photochemically-Mediated, Nickel-Catalyzed Synthesis ofOrganic letters · 2019Article
- Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future.Organometallics · 2019Article
- Article
- DFT Investigation of Suzuki-Miyaura Reactions with Aryl Sulfamates Using a Dialkylbiarylphosphine-Ligated Palladium Catalyst.Organometallics · 2017Article
- Well-defined nickel and palladium precatalysts for cross-coupling.Nature reviews. Chemistry · 2017Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Using a recently discovered precatalyst, the first Pd-catalyzed Suzuki-Miyaura reactions using aryl sulfamates that occur at room temperature are reported. In complementary work, it is demonstrated that a related precatalyst can facilitate the coupling of aryl silanolates, which are less toxic and reactive nucleophiles than boronic acids with aryl chlorides. By combining our results using modern electrophiles and nucleophiles, the first Hiyama-Denmark reactions using aryl sulfamates are reported.
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Registered trials
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