Cargando…

An expedient, mild and aqueous method for Suzuki–Miyaura diversification of (hetero)aryl halides or (poly)chlorinated pharmaceuticals

The development of mild, aqueous conditions for the cross-coupling of highly functionalized (hetero)aryl chlorides or bromides is attractive, enabling their functionalization and diversification. Herein, we report a general method for Suzuki–Miyaura cross-coupling at 37 °C in aqueous media in the pr...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sharma, Sunil V., Pubill-Ulldemolins, Cristina, Marelli, Enrico, Goss, Rebecca J. M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Royal Society of Chemistry 2021
Materias:	Chemistry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506956/ https://www.ncbi.nlm.nih.gov/pubmed/34745636 http://dx.doi.org/10.1039/d1qo00919b

Ejemplares similares

DNA-Compatible Suzuki-Miyaura Cross-Coupling Reaction of Aryl Iodides With (Hetero)Aryl Boronic Acids for DNA-Encoded Libraries
por: Siripuram, Vijay Kumar, et al.
Publicado: (2022)

Site-selective Suzuki–Miyaura coupling of heteroaryl halides – understanding the trends for pharmaceutically important classes
por: Almond-Thynne, Joshua, et al.
Publicado: (2017)

A novel 4-aminoantipyrine-Pd(II) complex catalyzes Suzuki–Miyaura cross-coupling reactions of aryl halides
por: Contreras-Celedón, Claudia Araceli, et al.
Publicado: (2014)

Substrate switchable Suzuki–Miyaura coupling for benzyl ester vs. benzyl halide
por: Ohsumi, Masato, et al.
Publicado: (2018)

Mild Palladium-Catalyzed Cyanation of (Hetero)aryl Halides and Triflates in Aqueous Media
por: Cohen, Daniel T., et al.
Publicado: (2015)

Heck Diversification of Indole‐Based Substrates under Aqueous Conditions: From Indoles to Unprotected Halo‐tryptophans and Halo‐tryptophans in Natural Product Derivatives
por: Pubill‐Ulldemolins, Cristina, et al.
Publicado: (2019)

Suzuki-Miyaura Coupling Enabled by Aryl to Vinyl 1,4-Palladium Migration
por: Li, Meng-Yao, et al.
Publicado: (2020)

Cobalt‐Catalyzed Suzuki Biaryl Coupling of Aryl Halides
por: Asghar, Soneela, et al.
Publicado: (2017)

Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates
por: Schäfer, Philipp, et al.
Publicado: (2017)

Efficient Synthesis of Unprotected C-5-Aryl/Heteroaryl-2'-deoxyuridine via a Suzuki-Miyaura Reaction in Aqueous Media
por: Fresneau, Nathalie, et al.
Publicado: (2012)

Partition of the Reactive Species of the Suzuki–Miyaura Reaction between Aqueous and Micellar Environments
por: Ranaudo, Anna, et al.
Publicado: (2022)

An Efficient Synthesis of Aryl-Substituted Pyrroles by the Suzuki–Miyaura Coupling Reaction of SEM-Protected Pyrroles
por: Cui, Keli, et al.
Publicado: (2019)

trans-Dichlorobis(XPhos)palladium(II) Precatalyst for Suzuki–Miyaura Cross-Coupling Reactions of Aryl/Vinyl Sulfonates/Halides: Scope, Mechanistic Study, and Synthetic Applications
por: Sirindil, Fatih, et al.
Publicado: (2021)

Pyrimidyl formamidine palladium(II) complex as a nanocatalyst for aqueous Suzuki-Miyaura coupling
por: Khormi, Afaf Y., et al.
Publicado: (2019)

Application of the Suzuki-Miyaura Reaction in the Synthesis of Flavonoids
por: Selepe, Mamoalosi A., et al.
Publicado: (2013)

Author Correction: Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates
por: Schäfer, Philipp, et al.
Publicado: (2018)

Cobalt-catalyzed aminocarbonylation of (hetero)aryl halides promoted by visible light
por: Veatch, Alexander M., et al.
Publicado: (2020)

Enhanced Aqueous Suzuki–Miyaura Coupling Allows Site-Specific Polypeptide (18)F-Labeling
por: Gao, Zhanghua, et al.
Publicado: (2013)

Functionalization of Framboidal Phenylboronic Acid-Containing Nanoparticles via Aqueous Suzuki–Miyaura Coupling Reactions
por: van der Vlies, André J., et al.
Publicado: (2023)

New biomaterials for Ni biosorption turned into catalysts for Suzuki–Miyaura cross coupling of aryl iodides in green conditions
por: Cases, Lucie, et al.
Publicado: (2021)

Suzuki–Miyaura coupling of arylboronic acids to gold(iii)
por: Maity, Ayan, et al.
Publicado: (2015)

Nickel-catalyzed Suzuki–Miyaura cross-couplings of aldehydes
por: Guo, Lin, et al.
Publicado: (2019)

Recent Developments in the Suzuki-Miyaura Reaction: 2010–2014
por: Maluenda, Irene, et al.
Publicado: (2015)

Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling
por: Matyugina, Elena S., et al.
Publicado: (2020)

Enantio‐ and Diastereoselective Suzuki–Miyaura Coupling with Racemic Bicycles
por: Goetzke, F. Wieland, et al.
Publicado: (2019)

Palladium-catalyzed Suzuki-Miyaura coupling of thioureas or thioamides
por: Mai, Shaoyu, et al.
Publicado: (2019)

Reusable Pd-PolyHIPE for Suzuki–Miyaura Coupling
por: Ravbar, Miha, et al.
Publicado: (2022)

Magnetic Lignosulfonate-Supported Pd Complex: Renewable Resource-Derived Catalyst for Aqueous Suzuki–Miyaura Reaction
por: Nasrollahzadeh, Mahmoud, et al.
Publicado: (2019)

Imine Palladacycles: Synthesis, Structural Analysis and Application in Suzuki–Miyaura Cross Coupling in Semi-Aqueous Media
por: Bermúdez-Puente, Brais, et al.
Publicado: (2022)

Cobalt‐Catalyzed Cross‐Coupling of Functionalized Alkylzinc Reagents with (Hetero)Aryl Halides
por: Lutter, Ferdinand H., et al.
Publicado: (2020)

Room-temperature borylation and one-pot two-step borylation/Suzuki–Miyaura cross-coupling reaction of aryl chlorides
por: Ji, Hong, et al.
Publicado: (2018)

Synthesis and Functionalization of Challenging meso-Substituted Aryl Bis-pocket Porphyrins Accessed via Suzuki–Miyaura Cross-Coupling
por: Droege, Daniel G., et al.
Publicado: (2022)

Suzuki–Miyaura cross-coupling optimization enabled by automated feedback
por: Reizman, Brandon J., et al.
Publicado: (2016)

Pd-Catalyzed Suzuki-Miyaura Cross-Coupling of Pentafluorophenyl Esters
por: Buchspies, Jonathan, et al.
Publicado: (2018)

Copper(i)-catalyzed sulfonylative Suzuki–Miyaura cross-coupling
por: Chen, Yiding, et al.
Publicado: (2017)

Suzuki–Miyaura Cross‐Coupling of Bromotryptophan Derivatives at Ambient Temperature
por: Dachwitz, Steffen, et al.
Publicado: (2020)

Peptide stapling by late-stage Suzuki–Miyaura cross-coupling
por: Gruß, Hendrik, et al.
Publicado: (2022)

The Direct Mechanocatalytic Suzuki–Miyaura Reaction of Small Organic Molecules
por: Pickhardt, Wilm, et al.
Publicado: (2022)

An Enantioselective Suzuki–Miyaura Coupling To Form Axially Chiral Biphenols
por: Pearce-Higgins, Robert, et al.
Publicado: (2022)

Iron(II) Active Species in Iron–Bisphosphine Catalyzed Kumada and Suzuki–Miyaura Cross-Couplings of Phenyl Nucleophiles and Secondary Alkyl Halides
por: Daifuku, Stephanie L., et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_ijf10j40n54j103u1cj563fu74