Literature DB >> 26184455

Iron-Catalyzed Cross-Coupling of Alkenyl Acetates.

Dominik Gärtner1, André Luiz Stein1, Sabine Grupe1, Johannes Arp1, Axel Jacobi von Wangelin2.   

Abstract

Stable C-O linkages are generally unreactive in cross-coupling reactions which mostly employ more electrophilic halides or activated esters (triflates, tosylates). Acetates are cheap and easily accessible electrophiles but have not been used in cross-couplings because the strong C-O bond and high propensity to engage in unwanted acetylation and deprotonation. Reported herein is a selective iron-catalyzed cross-coupling of diverse alkenyl acetates, and it operates under mild reaction conditions (0 °C, 2 h) with a ligand-free catalyst (1-2 mol%).
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Grignard reaction; alkenes; cross-coupling; enols; iron catalysis

Year:  2015        PMID: 26184455     DOI: 10.1002/anie.201504524

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  15 in total

1.  The N-Methylpyrrolidone (NMP) Effect in Iron-Catalyzed Cross-Coupling with Simple Ferric Salts and MeMgBr.

Authors:  Salvador B Muñoz; Stephanie L Daifuku; Jeffrey D Sears; Tessa M Baker; Stephanie H Carpenter; William W Brennessel; Michael L Neidig
Journal:  Angew Chem Int Ed Engl       Date:  2018-05-08       Impact factor: 15.336

2.  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

3.  Mechanism of the Bis(imino)pyridine-Iron-Catalyzed Hydromagnesiation of Styrene Derivatives.

Authors:  Peter G N Neate; Mark D Greenhalgh; William W Brennessel; Stephen P Thomas; Michael L Neidig
Journal:  J Am Chem Soc       Date:  2019-06-17       Impact factor: 15.419

4.  Additive and Counterion Effects in Iron-Catalyzed Reactions Relevant to C-C Bond Formation.

Authors:  Nikki J Bakas; Michael L Neidig
Journal:  ACS Catal       Date:  2021-06-29       Impact factor: 13.700

5.  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

6.  Iron-catalyzed Cross-Coupling of Propargyl Carboxylates and Grignard Reagents: Synthesis of Substituted Allenes.

Authors:  Simon N Kessler; Jan-E Bäckvall
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-17       Impact factor: 15.336

7.  A Synthesis of Substituted α-Allenols via Iron-Catalyzed Cross-Coupling of Propargyl Carboxylates with Grignard Reagents.

Authors:  Simon N Kessler; Fabian Hundemer; Jan-E Bäckvall
Journal:  ACS Catal       Date:  2016-09-28       Impact factor: 13.084

8.  Dilithium Amides as a Modular Bis-Anionic Ligand Platform for Iron-Catalyzed Cross-Coupling.

Authors:  Peter G N Neate; Bufan Zhang; Jessica Conforti; William W Brennessel; Michael L Neidig
Journal:  Org Lett       Date:  2021-07-26       Impact factor: 6.072

9.  Electronic Structure and Bonding in Iron(II) and Iron(I) Complexes Bearing Bisphosphine Ligands of Relevance to Iron-Catalyzed C-C Cross-Coupling.

Authors:  Jared L Kneebone; Valerie E Fleischauer; Stephanie L Daifuku; Ari A Shaps; Joseph M Bailey; Theresa E Iannuzzi; Michael L Neidig
Journal:  Inorg Chem       Date:  2015-12-14       Impact factor: 5.165

10.  Manganese(I)-Catalyzed C-H Activation: The Key Role of a 7-Membered Manganacycle in H-Transfer and Reductive Elimination.

Authors:  Nasiru P Yahaya; Kate M Appleby; Magdalene Teh; Conrad Wagner; Erik Troschke; Joshua T W Bray; Simon B Duckett; L Anders Hammarback; Jonathan S Ward; Jessica Milani; Natalie E Pridmore; Adrian C Whitwood; Jason M Lynam; Ian J S Fairlamb
Journal:  Angew Chem Int Ed Engl       Date:  2016-09-07       Impact factor: 15.336

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