Literature DB >> 23952217

Mechanism and selectivity in nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides.

Soumik Biswas1, Daniel J Weix.   

Abstract

The direct cross-coupling of two different electrophiles, such as an aryl halide with an alkyl halide, offers many advantages over conventional cross-coupling methods that require a carbon nucleophile. Despite its promise as a versatile synthetic strategy, a limited understanding of the mechanism and origin of cross selectivity has hindered progress in reaction development and design. Herein, we shed light on the mechanism for the nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides and demonstrate that the selectivity arises from an unusual catalytic cycle that combines both polar and radical steps to form the new C-C bond.

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Year:  2013        PMID: 23952217      PMCID: PMC3946589          DOI: 10.1021/ja407589e

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  45 in total

1.  Aryl-aryl bond formation one century after the discovery of the Ullmann reaction.

Authors:  Jwanro Hassan; Marc Sévignon; Christel Gozzi; Emmanuelle Schulz; Marc Lemaire
Journal:  Chem Rev       Date:  2002-05       Impact factor: 60.622

Review 2.  Radicals in transition metal catalyzed reactions? transition metal catalyzed radical reactions? - a fruitful interplay anyway: part 2. Radical catalysis by group 8 and 9 elements.

Authors:  Ullrich Jahn
Journal:  Top Curr Chem       Date:  2012

3.  Theoretical study on the mechanism of Ni-catalyzed alkyl-alkyl Suzuki cross-coupling.

Authors:  Zhe Li; Yuan-Ye Jiang; Yao Fu
Journal:  Chemistry       Date:  2012-02-28       Impact factor: 5.236

4.  Nickel-Catalyzed Direct Electrochemical Cross-Coupling between Aryl Halides and Activated Alkyl Halides.

Authors:  Muriel Durandetti; Jean-Yves Nédélec; Jacques Périchon
Journal:  J Org Chem       Date:  1996-03-08       Impact factor: 4.354

Review 5.  Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals.

Authors:  Javier Magano; Joshua R Dunetz
Journal:  Chem Rev       Date:  2011-03-09       Impact factor: 60.622

6.  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

7.  Scope of the palladium-catalyzed aryl borylation utilizing bis-boronic acid.

Authors:  Gary A Molander; Sarah L J Trice; Steven M Kennedy; Spencer D Dreher; Matthew T Tudge
Journal:  J Am Chem Soc       Date:  2012-07-06       Impact factor: 15.419

8.  Selectivity in metal-catalyzed carbon-carbon bond cleavage of alkylidenecyclopropanes.

Authors:  Ahmad Masarwa; Ilan Marek
Journal:  Chemistry       Date:  2010-08-23       Impact factor: 5.236

9.  Ketone formation via mild nickel-catalyzed reductive coupling of alkyl halides with aryl acid chlorides.

Authors:  Fan Wu; Wenbin Lu; Qun Qian; Qinghua Ren; Hegui Gong
Journal:  Org Lett       Date:  2012-05-31       Impact factor: 6.005

10.  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

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  97 in total

1.  Nickel-Catalyzed Asymmetric Reductive Cross-Coupling To Access 1,1-Diarylalkanes.

Authors:  Kelsey E Poremba; Nathaniel T Kadunce; Naoyuki Suzuki; Alan H Cherney; Sarah E Reisman
Journal:  J Am Chem Soc       Date:  2017-04-13       Impact factor: 15.419

2.  The High Chemofidelity of Metal-Catalyzed Hydrogen Atom Transfer.

Authors:  Samantha A Green; Steven W M Crossley; Jeishla L M Matos; Suhelen Vásquez-Céspedes; Sophia L Shevick; Ryan A Shenvi
Journal:  Acc Chem Res       Date:  2018-11-08       Impact factor: 22.384

3.  Synthesis of Tetrasubstituted Alkenes by Tandem Metallacycle Formation/Cross-Electrophile Coupling.

Authors:  Kirk W Shimkin; John Montgomery
Journal:  J Am Chem Soc       Date:  2018-05-31       Impact factor: 15.419

4.  A Radical Approach to Anionic Chemistry: Synthesis of Ketones, Alcohols, and Amines.

Authors:  Shengyang Ni; Natalia M Padial; Cian Kingston; Julien C Vantourout; Daniel C Schmitt; Jacob T Edwards; Monika M Kruszyk; Rohan R Merchant; Pavel K Mykhailiuk; Brittany B Sanchez; Shouliang Yang; Matthew A Perry; Gary M Gallego; James J Mousseau; Michael R Collins; Robert J Cherney; Pavlo S Lebed; Jason S Chen; Tian Qin; Phil S Baran
Journal:  J Am Chem Soc       Date:  2019-04-16       Impact factor: 15.419

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

Authors:  Keywan A Johnson; Soumik Biswas; Daniel J Weix
Journal:  Chemistry       Date:  2016-04-28       Impact factor: 5.236

6.  Breaking Amides using Nickel Catalysis.

Authors:  Jacob E Dander; Neil K Garg
Journal:  ACS Catal       Date:  2017-01-06       Impact factor: 13.084

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

Authors:  Alexander C Wotal; Donald C Batesky; Daniel J Weix
Journal:  Organic Synth       Date:  2016-02-22

8.  Stereospecific Synthesis of E-Alkenes through Anti-Markovnikov Hydroalkylation of Terminal Alkynes.

Authors:  Avijit Hazra; Jason Chen; Gojko Lalic
Journal:  J Am Chem Soc       Date:  2019-08-02       Impact factor: 15.419

9.  Nickel/Photoredox-Catalyzed Amidation via Alkylsilicates and Isocyanates.

Authors:  Shuai Zheng; David N Primer; Gary A Molander
Journal:  ACS Catal       Date:  2017-10-25       Impact factor: 13.084

10.  Nickel-Catalyzed Asymmetric Reductive Cross-Coupling between Heteroaryl Iodides and α-Chloronitriles.

Authors:  Nathaniel T Kadunce; Sarah E Reisman
Journal:  J Am Chem Soc       Date:  2015-08-13       Impact factor: 15.419

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