Literature DB >> 16438528

Iron-phosphine, -phosphite, -arsine, and -carbene catalysts for the coupling of primary and secondary alkyl halides with aryl Grignard reagents.

Robin B Bedford1, Michael Betham, Duncan W Bruce, Andreas A Danopoulos, Robert M Frost, Michael Hird.   

Abstract

Simple catalysts formed in situ from iron chloride and a wide range of monodentate and bidentate phosphines and arsines have been screened in the coupling of alkyl halides bearing beta-hydrogens with aryl Grignard reagents. The best of these show excellent activity, as do catalysts formed in situ with monodentate trialkyl and triaryl phosphite ligands. N-heterocyclic carbene-based precatalysts, either preformed or made in situ, also show excellent performance.

Entities:  

Year:  2006        PMID: 16438528     DOI: 10.1021/jo052250+

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  24 in total

1.  Stereospecific cross-coupling of secondary alkyl β-trifluoroboratoamides.

Authors:  Deidre L Sandrock; Ludivine Jean-Gérard; Cheng-yi Chen; Spencer D Dreher; Gary A Molander
Journal:  J Am Chem Soc       Date:  2010-11-15       Impact factor: 15.419

2.  A Physical-Inorganic Approach for the Elucidation of Active Iron Species and Mechanism in Iron-Catalyzed Cross-Coupling.

Authors:  Stephanie H Carpenter; Michael L Neidig
Journal:  Isr J Chem       Date:  2017-08-24       Impact factor: 3.333

3.  Intermediates and Reactivity in Iron-Catalyzed Cross-Couplings of Alkynyl Grignards with Alkyl Halides.

Authors:  Jared L Kneebone; William W Brennessel; Michael L Neidig
Journal:  J Am Chem Soc       Date:  2017-05-16       Impact factor: 15.419

4.  Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.

Authors:  Scott E Denmark; Alexander J Cresswell
Journal:  J Org Chem       Date:  2013-11-20       Impact factor: 4.354

5.  Organozinc Chemistry Enabled by Micellar Catalysis. Palladium-Catalyzed Cross-Couplings between Alkyl and Aryl Bromides in Water at Room Temperature.

Authors:  Christophe Duplais; Arkady Krasovskiy; Bruce H Lipshutz
Journal:  Organometallics       Date:  2011-11-21       Impact factor: 3.876

6.  Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides--reaction discovery using parallel microscale experimentation.

Authors:  Spencer D Dreher; Peter G Dormer; Deidre L Sandrock; Gary A Molander
Journal:  J Am Chem Soc       Date:  2008-06-27       Impact factor: 15.419

7.  Development and Evolution of Mechanistic Understanding in Iron-Catalyzed Cross-Coupling.

Authors:  Michael L Neidig; Stephanie H Carpenter; Daniel J Curran; Joshua C DeMuth; Valerie E Fleischauer; Theresa E Iannuzzi; Peter G N Neate; Jeffrey D Sears; Nikki J Wolford
Journal:  Acc Chem Res       Date:  2018-12-28       Impact factor: 22.384

8.  Intermediates and Mechanism in Iron-Catalyzed Cross-Coupling.

Authors:  Jeffrey D Sears; Peter G N Neate; Michael L Neidig
Journal:  J Am Chem Soc       Date:  2018-09-18       Impact factor: 15.419

9.  Oxidative Addition of Aryl and Alkyl Halides to a Reduced Iron Pincer Complex.

Authors:  Stephan M Rummelt; Paul O Peterson; Hongyu Zhong; Paul J Chirik
Journal:  J Am Chem Soc       Date:  2021-04-08       Impact factor: 15.419

10.  A TMEDA-Iron Adduct Reaction Manifold in Iron-Catalyzed C(sp2 )-C(sp3 ) Cross-Coupling Reactions.

Authors:  Nikki J Bakas; Jeffrey D Sears; William W Brennessel; Michael L Neidig
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-18       Impact factor: 15.336

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