Literature DB >> 31741548

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

Louis-Charles Campeau1, Nilay Hazari2.   

Abstract

Cross-coupling reactions, which were discovered almost 50 years ago, are widely used in both industry and academia. Even though cross-coupling reactions now represent mature technology, there is still a significant amount of research in this area that aims to improve the scope of these reactions, develop more efficient catalysts, and make reactions more practical. In this tutorial, a brief background to cross-coupling reactions is provided, and then the major advances in cross-coupling research over the last 20 years are described. These include the development of improved ligands and precatalysts for cross-coupling and the extension of cross-coupling reactions to a much wider range of electrophiles. For example, cross-coupling reactions are now common with sp3-hybridized electrophiles as well as ester, amide, ether, and aziridine substrates. For many of these more modern substrates, traditional palladium-based catalysts are less efficient than systems based on first-row transition metals such as nickel. Conventional cross-coupling reactions have also inspired the development of a range of related reactions, such as cross-electrophile and decarboxylative couplings as well as couplings based on metallaphotoredox chemistry. The development of these new reactions is probably at the same stage as traditional cross-coupling reactions 30 years ago, and this tutorial highlights how many of the same strategies used to improve cross-coupling reactions may also be applicable to making the new reactions more practical.

Entities:  

Year:  2018        PMID: 31741548      PMCID: PMC6860378          DOI: 10.1021/acs.organomet.8b00720

Source DB:  PubMed          Journal:  Organometallics        ISSN: 0276-7333            Impact factor:   3.876


  249 in total

1.  Cross coupling.

Authors:  Stephen L Buchwald
Journal:  Acc Chem Res       Date:  2008-11-18       Impact factor: 22.384

2.  Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design.

Authors:  Marc Lafrance; Keith Fagnou
Journal:  J Am Chem Soc       Date:  2006-12-27       Impact factor: 15.419

3.  Decarbonylative Diaryl Ether Synthesis by Pd and Ni Catalysis.

Authors:  Ryosuke Takise; Ryota Isshiki; Kei Muto; Kenichiro Itami; Junichiro Yamaguchi
Journal:  J Am Chem Soc       Date:  2017-02-22       Impact factor: 15.419

4.  Direct Aldehyde C-H Arylation and Alkylation via the Combination of Nickel, Hydrogen Atom Transfer, and Photoredox Catalysis.

Authors:  Xiaheng Zhang; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2017-08-14       Impact factor: 15.419

5.  Cross-coupling of aryl/alkenyl ethers with aryl Grignard reagents through nickel-catalyzed C-O activation.

Authors:  Lan-Gui Xie; Zhong-Xia Wang
Journal:  Chemistry       Date:  2011-03-01       Impact factor: 5.236

6.  Nickel-Catalyzed Diaryl Ketone Synthesis by N-C Cleavage: Direct Negishi Cross-Coupling of Primary Amides by Site-Selective N,N-Di-Boc Activation.

Authors:  Shicheng Shi; Michal Szostak
Journal:  Org Lett       Date:  2016-11-08       Impact factor: 6.005

Review 7.  Rhodium-catalyzed C-C bond formation via heteroatom-directed C-H bond activation.

Authors:  Denise A Colby; Robert G Bergman; Jonathan A Ellman
Journal:  Chem Rev       Date:  2010-02-10       Impact factor: 60.622

8.  Rapidly Activating Pd-Precatalyst for Suzuki-Miyaura and Buchwald-Hartwig Couplings of Aryl Esters.

Authors:  Amira H Dardir; Patrick R Melvin; Ryan M Davis; Nilay Hazari; Megan Mohadjer Beromi
Journal:  J Org Chem       Date:  2017-12-12       Impact factor: 4.354

9.  New ligands for nickel catalysis from diverse pharmaceutical heterocycle libraries.

Authors:  Eric C Hansen; Dylan J Pedro; Alexander C Wotal; Nicholas J Gower; Jade D Nelson; Stephane Caron; Daniel J Weix
Journal:  Nat Chem       Date:  2016-08-08       Impact factor: 24.427

10.  Suzuki-Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C-N and C-O bonds.

Authors:  Peng Lei; Guangrong Meng; Shicheng Shi; Yun Ling; Jie An; Roman Szostak; Michal Szostak
Journal:  Chem Sci       Date:  2017-08-01       Impact factor: 9.825

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  20 in total

1.  Differences in the Performance of Allyl Based Palladium Precatalysts for Suzuki-Miyaura Reactions.

Authors:  Matthew R Espinosa; Angelino Doppiu; Nilay Hazari
Journal:  Adv Synth Catal       Date:  2020-08-27       Impact factor: 5.837

2.  Direct Observation of Transmetalation from a Neutral Boronate Ester to a Pyridine(diimine) Iron Alkoxide.

Authors:  Paul O Peterson; Stephan M Rummelt; Bradley M Wile; S Chantal E Stieber; Hongyu Zhong; Paul J Chirik
Journal:  Organometallics       Date:  2019-12-23       Impact factor: 3.876

3.  Single-Micelle and Single-Zinc-Particle Imaging Provides Insights into the Physical Processes Underpinning Organozinc Reactions in Water.

Authors:  Hannah Peacock; Suzanne A Blum
Journal:  J Am Chem Soc       Date:  2022-02-14       Impact factor: 15.419

Review 4.  Homogeneous Organic Electron Donors in Nickel-Catalyzed Reductive Transformations.

Authors:  David J Charboneau; Nilay Hazari; Haotian Huang; Mycah R Uehling; Susan L Zultanski
Journal:  J Org Chem       Date:  2022-06-07       Impact factor: 4.198

5.  Perfluorinated phosphine and hybrid P-O ligands for Pd catalysed C-C bond forming reactions in solution and on Teflon supports.

Authors:  Farzana Begum; Muhammad Ikram; Brendan Twamley; Robert J Baker
Journal:  RSC Adv       Date:  2019-09-13       Impact factor: 4.036

6.  Palladium-catalyzed decarbonylative Suzuki-Miyaura cross-coupling of amides by carbon-nitrogen bond activation.

Authors:  Tongliang Zhou; Chong-Lei Ji; Xin Hong; Michal Szostak
Journal:  Chem Sci       Date:  2019-09-03       Impact factor: 9.825

7.  Efficient Pd-Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents.

Authors:  Thorsten Scherpf; Henning Steinert; Angela Großjohann; Katharina Dilchert; Jens Tappen; Ilja Rodstein; Viktoria H Gessner
Journal:  Angew Chem Int Ed Engl       Date:  2020-09-08       Impact factor: 15.336

8.  Cobalt-Catalyzed C(sp2)-C(sp3) Suzuki-Miyaura Cross Coupling.

Authors:  Jacob R Ludwig; Eric M Simmons; Steven R Wisniewski; Paul J Chirik
Journal:  Org Lett       Date:  2020-09-30       Impact factor: 6.005

9.  Advances in Cross-Coupling Reactions.

Authors:  José Pérez Sestelo; Luis A Sarandeses
Journal:  Molecules       Date:  2020-10-01       Impact factor: 4.411

10.  Photoactive electron donor-acceptor complex platform for Ni-mediated C(sp3)-C(sp2) bond formation.

Authors:  Lisa Marie Kammer; Shorouk O Badir; Ren-Ming Hu; Gary A Molander
Journal:  Chem Sci       Date:  2021-03-05       Impact factor: 9.825

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