Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Highly reactive, single-component nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides.

Literature DB >> 23136047

Highly reactive, single-component nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides.

Shaozhong Ge¹, John F Hartwig.

Abstract

Entities: Chemical Disease Gene

Mesh：

Substances：

Year: 2012 PMID： 23136047 PMCID： PMC3613336 DOI： 10.1002/anie.201207428

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

× No keyword cloud information.

21 in total

1. The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

Authors: Stephen D Roughley; Allan M Jordan
Journal: J Med Chem Date: 2011-05-02 Impact factor: 7.446

2. Nickel-catalyzed asymmetric α-arylation and heteroarylation of ketones with chloroarenes: effect of halide on selectivity, oxidation state, and room-temperature reactions.

Authors: Shaozhong Ge; John F Hartwig
Journal: J Am Chem Soc Date: 2011-09-27 Impact factor: 15.419

3. trans-Chloro(1-naphthyl)bis(triphenylphosphine)nickel(II)/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates at room temperature.

Authors: Pawaret Leowanawat; Na Zhang; Mehtap Safi; David J Hoffman; Miriam C Fryberger; Aiswaria George; Virgil Percec
Journal: J Org Chem Date: 2012-03-07 Impact factor: 4.354

4. Ni(COD)2/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates in THF at room temperature.

Authors: Pawaret Leowanawat; Na Zhang; Ana-Maria Resmerita; Brad M Rosen; Virgil Percec
Journal: J Org Chem Date: 2011-11-16 Impact factor: 4.354

5. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.

Authors: Tom Kinzel; Yong Zhang; Stephen L Buchwald
Journal: J Am Chem Soc Date: 2010-10-13 Impact factor: 15.419

6. Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates.

Authors: Kyle W Quasdorf; Michelle Riener; Krastina V Petrova; Neil K Garg
Journal: J Am Chem Soc Date: 2009-12-16 Impact factor: 15.419

7. N,N-diethyl O-carbamate: directed metalation group and orthogonal Suzuki-Miyaura cross-coupling partner.

Authors: Aurora Antoft-Finch; Tom Blackburn; Victor Snieckus
Journal: J Am Chem Soc Date: 2009-12-16 Impact factor: 15.419

8. NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.

Authors: Virgil Percec; Geoffrey M Golding; Jan Smidrkal; Oliver Weichold
Journal: J Org Chem Date: 2004-05-14 Impact factor: 4.354

9. Nickel-catalyzed cross-coupling of aryl methyl ethers with aryl boronic esters.

Authors: Mamoru Tobisu; Toshiaki Shimasaki; Naoto Chatani
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

10. Cross-coupling reactions of aryl pivalates with boronic acids.

Authors: Kyle W Quasdorf; Xia Tian; Neil K Garg
Journal: J Am Chem Soc Date: 2008-10-08 Impact factor: 15.419

24 in total

1. Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species.

Authors: Megan Mohadjer Beromi; Ainara Nova; David Balcells; Ann M Brasacchio; Gary W Brudvig; Louise M Guard; Nilay Hazari; David J Vinyard
Journal: J Am Chem Soc Date: 2017-01-10 Impact factor: 15.419

2. Well-defined nickel and palladium precatalysts for cross-coupling.

Authors: Nilay Hazari; Patrick R Melvin; Megan Mohadjer Beromi
Journal: Nat Rev Chem Date: 2017-03-01 Impact factor: 34.035

3. Modifications to the Aryl Group of dppf-Ligated Ni σ‑Aryl Precatalysts: Impact on Speciation and Catalytic Activity in Suzuki-Miyaura Coupling Reactions.

Authors: Megan Mohadjer Beromi; Gourab Banerjee; Gary W Brudvig; David J Charboneau; Nilay Hazari; Hannah M C Lant; Brandon Q Mercado
Journal: Organometallics Date: 2018-10-16 Impact factor: 3.876

Highly reactive, single-component nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides.

1. The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

2. Nickel-catalyzed asymmetric α-arylation and heteroarylation of ketones with chloroarenes: effect of halide on selectivity, oxidation state, and room-temperature reactions.

3. trans-Chloro(1-naphthyl)bis(triphenylphosphine)nickel(II)/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates at room temperature.

4. Ni(COD)2/PCy3 catalyzed cross-coupling of aryl and heteroaryl neopentylglycolboronates with aryl and heteroaryl mesylates and sulfamates in THF at room temperature.

5. A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.

6. Suzuki-Miyaura coupling of aryl carbamates, carbonates, and sulfamates.

7. N,N-diethyl O-carbamate: directed metalation group and orthogonal Suzuki-Miyaura cross-coupling partner.

8. NiCl(2)(dppe)-catalyzed cross-coupling of aryl mesylates, arenesulfonates, and halides with arylboronic acids.

9. Nickel-catalyzed cross-coupling of aryl methyl ethers with aryl boronic esters.

10. Cross-coupling reactions of aryl pivalates with boronic acids.

1. Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species.

2. Well-defined nickel and palladium precatalysts for cross-coupling.

3. Modifications to the Aryl Group of dppf-Ligated Ni σ‑Aryl Precatalysts: Impact on Speciation and Catalytic Activity in Suzuki-Miyaura Coupling Reactions.

4. A modular, air-stable nickel precatalyst.

5. Nickel-Catalyzed Stille Cross Coupling of C-O Electrophiles.

6. Benchtop Delivery of Ni(cod)2 using Paraffin Capsules.

7. Nickel-catalyzed Suzuki-Miyaura couplings in green solvents.

8. Nanonickel-catalyzed Suzuki-Miyaura cross-couplings in water.

Review 9. Recent advances in homogeneous nickel catalysis.

10. Enantioselective, nickel-catalyzed Suzuki cross-coupling of quinolinium ions.