Literature DB >> 24828188

Recent advances in homogeneous nickel catalysis.

Sarah Z Tasker1, Eric A Standley1, Timothy F Jamison2.   

Abstract

Tremendous advances have been made in nickel catalysis over the past decade. Several key properties of nickel, such as facile oxidative addition and ready access to multiple oxidation states, have allowed the development of a broad range of innovative reactions. In recent years, these properties have been increasingly understood and used to perform transformations long considered exceptionally challenging. Here we discuss some of the most recent and significant developments in homogeneous nickel catalysis, with an emphasis on both synthetic outcome and mechanism.

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Year:  2014        PMID: 24828188      PMCID: PMC4344729          DOI: 10.1038/nature13274

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  79 in total

1.  Interactions of aziridines with nickel complexes: oxidative-addition and reductive-elimination reactions that break and make C-N bonds.

Authors:  Beatrice L Lin; Christopher R Clough; Gregory L Hillhouse
Journal:  J Am Chem Soc       Date:  2002-03-27       Impact factor: 15.419

2.  A general strategy for regiocontrol in nickel-catalyzed reductive couplings of aldehydes and alkynes.

Authors:  Hasnain A Malik; Grant J Sormunen; John Montgomery
Journal:  J Am Chem Soc       Date:  2010-05-12       Impact factor: 15.419

3.  Isolation, structure, and reactivity of an arylnickel(II) pivalate complex in catalytic C-H/C-O biaryl coupling.

Authors:  Kei Muto; Junichiro Yamaguchi; Aiwen Lei; Kenichiro Itami
Journal:  J Am Chem Soc       Date:  2013-10-29       Impact factor: 15.419

4.  A structurally rigid bis(amido) ligand framework in low-coordinate Ni(I), Ni(II), and Ni(III) analogues provides access to a Ni(III) methyl complex via oxidative addition.

Authors:  Michael I Lipschutz; Xinzheng Yang; Ruchira Chatterjee; T Don Tilley
Journal:  J Am Chem Soc       Date:  2013-10-03       Impact factor: 15.419

5.  Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

Authors:  Kyle W Quasdorf; Aurora Antoft-Finch; Peng Liu; Amanda L Silberstein; Anna Komaromi; Tom Blackburn; Stephen D Ramgren; K N Houk; Victor Snieckus; Neil K Garg
Journal:  J Am Chem Soc       Date:  2011-04-01       Impact factor: 15.419

6.  Ligand-switchable directing effects of tethered alkenes in nickel-catalyzed additions to alkynes.

Authors:  Karen M Miller; Timothy F Jamison
Journal:  J Am Chem Soc       Date:  2004-12-01       Impact factor: 15.419

7.  Nickel-catalyzed direct alkylation of C-H bonds in benzamides and acrylamides with functionalized alkyl halides via bidentate-chelation assistance.

Authors:  Yoshinori Aihara; Naoto Chatani
Journal:  J Am Chem Soc       Date:  2013-04-01       Impact factor: 15.419

8.  Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates.

Authors:  Josep Cornella; Enrique Gómez-Bengoa; Ruben Martin
Journal:  J Am Chem Soc       Date:  2013-01-23       Impact factor: 15.419

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.  Traceless directing group for stereospecific nickel-catalyzed alkyl-alkyl cross-coupling reactions.

Authors:  Margaret A Greene; Ivelina M Yonova; Florence J Williams; Elizabeth R Jarvo
Journal:  Org Lett       Date:  2012-05-08       Impact factor: 6.005

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  230 in total

1.  Nickel-Catalyzed Reductive [2+2] Cycloaddition of Alkynes.

Authors:  Santiago Cañellas; John Montgomery; Miquel À Pericàs
Journal:  J Am Chem Soc       Date:  2018-12-10       Impact factor: 15.419

2.  Organic chemistry: Light opens pathways for nickel catalysis.

Authors:  John J Murphy; Paolo Melchiorre
Journal:  Nature       Date:  2015-08-12       Impact factor: 49.962

3.  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

4.  Palladium Catalyzed Arylation and Benzylation of Nitroarenes Using Aryl Sulfonates and Benzyl Acetates.

Authors:  Zubaoyi Yi; Yodit Aschenaki; Ryan Daley; Stephen Davick; Abigail Schnaith; Rylee Wander; Dipannita Kalyani
Journal:  J Org Chem       Date:  2017-06-15       Impact factor: 4.354

5.  Nickel Catalysis: Synergy between Method Development and Total Synthesis.

Authors:  Eric A Standley; Sarah Z Tasker; Kim L Jensen; Timothy F Jamison
Journal:  Acc Chem Res       Date:  2015-04-23       Impact factor: 22.384

6.  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

7.  Nickel-Catalyzed Asymmetric Kumada Cross-Coupling of Symmetric Cyclic Sulfates.

Authors:  Meredith S Eno; Alexander Lu; James P Morken
Journal:  J Am Chem Soc       Date:  2016-06-16       Impact factor: 15.419

8.  Synthesis of Alkyl Halides from Aldehydes via Deformylative Halogenation.

Authors:  Shengzong Liang; Tatsuya Kumon; Ricardo A Angnes; Melissa Sanchez; Bo Xu; Gerald B Hammond
Journal:  Org Lett       Date:  2019-05-03       Impact factor: 6.005

9.  Nickel-Catalyzed Mizoroki-Heck-Type Reactions of Unactivated Alkyl Bromides.

Authors:  Megan R Kwiatkowski; Erik J Alexanian
Journal:  Angew Chem Int Ed Engl       Date:  2018-11-20       Impact factor: 15.336

10.  Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.

Authors:  Sarah M Pound; Mary P Watson
Journal:  Chem Commun (Camb)       Date:  2018-10-30       Impact factor: 6.222

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