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Literature DB >> 24817773

Nickel-Catalyzed Cross-Coupling of Aryl Halides with Alkyl Halides: Ethyl 4-(4-(4-methylphenylsulfonamido)-phenyl)butanoate.

Daniel A Everson¹, David T George¹, Daniel J Weix¹, Jonas F Buergler¹, John L Wood¹.

Abstract

Entities: Chemical Disease Gene Species

Year: 2013 PMID： 24817773 PMCID： PMC4012698 DOI： 10.15227/orgsyn.090.0200

Source DB: PubMed Journal: Organic Synth ISSN： 0078-6209

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17 in total

1. Direct method for carbon-carbon bond formation: the functional group tolerant cobalt-catalyzed alkylation of aryl halides.

Authors: Muriel Amatore; Corinne Gosmini
Journal: Chemistry Date: 2010-05-25 Impact factor: 5.236

2. Catalysts for cross-coupling reactions with non-activated alkyl halides.

Authors: Anja C Frisch; Matthias Beller
Journal: Angew Chem Int Ed Engl Date: 2005-01-21 Impact factor: 15.336

3. Identification of novel glycine sulfonamide antagonists for the EP1 receptor.

Authors: Stephen C McKeown; Adrian Hall; Richard Blunt; Susan H Brown; Iain P Chessell; Anita Chowdhury; Gerard M P Giblin; Mark P Healy; Matthew R Johnson; Olivier Lorthioir; Anton D Michel; Alan Naylor; Xiao Lewell; Shilina Roman; Stephen P Watson; Wendy J Winchester; Richard J Wilson
Journal: Bioorg Med Chem Lett Date: 2006-12-22 Impact factor: 2.823

Review 4. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors: Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal: Chem Rev Date: 2011-02-14 Impact factor: 60.622

5. Nickel-mediated inter- and intramolecular reductive cross-coupling of unactivated alkyl bromides and aryl iodides at room temperature.

Authors: Chang-Song Yan; Yu Peng; Xiao-Bo Xu; Ya-Wen Wang
Journal: Chemistry Date: 2012-03-30 Impact factor: 5.236

6. Nickel-catalyzed reductive coupling of aryl halides with secondary alkyl bromides and allylic acetate.

Authors: Shulin Wang; Qun Qian; Hegui Gong
Journal: Org Lett Date: 2012-06-14 Impact factor: 6.005

7. Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents.

Authors: Arkady Krasovskiy; Christophe Duplais; Bruce H Lipshutz
Journal: J Am Chem Soc Date: 2009-11-04 Impact factor: 15.419

8. Nickel-catalyzed reductive cross-coupling of aryl halides with alkyl halides.

Authors: Daniel A Everson; Ruja Shrestha; Daniel J Weix
Journal: J Am Chem Soc Date: 2010-01-27 Impact factor: 15.419

9. Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.

Authors: Nicolas Fleury-Brégeot; Marc Presset; Floriane Beaumard; Virginie Colombel; Daniel Oehlrich; Frederik Rombouts; Gary A Molander
Journal: J Org Chem Date: 2012-11-06 Impact factor: 4.354

10. Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides.

Authors: Daniel A Everson; Brittany A Jones; Daniel J Weix
Journal: J Am Chem Soc Date: 2012-03-30 Impact factor: 15.419

11 in total

Nickel-Catalyzed Cross-Coupling of Aryl Halides with Alkyl Halides: Ethyl 4-(4-(4-methylphenylsulfonamido)-phenyl)butanoate.

1. Direct method for carbon-carbon bond formation: the functional group tolerant cobalt-catalyzed alkylation of aryl halides.

2. Catalysts for cross-coupling reactions with non-activated alkyl halides.

3. Identification of novel glycine sulfonamide antagonists for the EP1 receptor.

Review 4. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

5. Nickel-mediated inter- and intramolecular reductive cross-coupling of unactivated alkyl bromides and aryl iodides at room temperature.

6. Nickel-catalyzed reductive coupling of aryl halides with secondary alkyl bromides and allylic acetate.

7. Zn-mediated, Pd-catalyzed cross-couplings in water at room temperature without prior formation of organozinc reagents.

8. Nickel-catalyzed reductive cross-coupling of aryl halides with alkyl halides.

9. Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: access to aryl/heteroarylethyloxy motifs.

10. Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides.

1. Nickel-catalyzed cross-electrophile coupling of 2-chloropyridines with alkyl bromides.

2. Cross-Electrophile Coupling of Vinyl Halides with Alkyl Halides.

3. Cross-Coupling and Related Reactions: Connecting Past Success to the Development of New Reactions for the Future.

4. Nickel-Catalyzed Synthesis of Ketones from Alkyl Halides and Acid Chlorides: Preparation of Ethyl 4-Oxododecanoate.

5. Nickel-catalyzed regiodivergent opening of epoxides with aryl halides: co-catalysis controls regioselectivity.

6. Substituted 2,2'-bipyridines by nickel-catalysis: 4,4'-di-tert-butyl-2,2'-bipyridine.

7. Methods and Mechanisms for Cross-Electrophile Coupling of Csp(2) Halides with Alkyl Electrophiles.

8. Stoichiometric Reactions of Acylnickel(II) Complexes with Electrophiles and the Catalytic Synthesis of Ketones.

9. ChemBead Enabled High-Throughput Cross-Electrophile Coupling Reveals a New Complementary Ligand.

10. Cross-electrophile coupling: principles of reactivity and selectivity.