Literature DB >> 24273111

Organic electron donors as powerful single-electron reducing agents in organic synthesis.

Julie Broggi1, Thierry Terme, Patrice Vanelle.   

Abstract

One-electron reduction is commonly used in organic chemistry for the formation of radicals by the stepwise transfer of one or two electrons from a donor to an organic substrate. Besides metallic reagents, single-electron reducers based on neutral organic molecules have emerged as an attractive novel source of reducing electrons. The past 20 years have seen the blossoming of a particular class of organic reducing agents, the electron-rich olefins, and their application in organic synthesis. This Review gives an overview of the different types of organic donors and their specific characteristics in organic transformations.
Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  electron transfer; electron-rich olefins; organic electron donors; reduction

Mesh:

Substances:

Year:  2013        PMID: 24273111     DOI: 10.1002/anie.201209060

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


  27 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.  Studies toward the oxidative and reductive activation of C-S bonds in 2'-S-aryl-2'-thiouridine derivatives.

Authors:  Ramanjaneyulu Rayala; Alain Giuglio-Tonolo; Julie Broggi; Thierry Terme; Patrice Vanelle; Patricia Theard; Maurice Médebielle; Stanislaw F Wnuk
Journal:  Tetrahedron       Date:  2016-04-21       Impact factor: 2.457

3.  Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling.

Authors:  David J Charboneau; Haotian Huang; Emily L Barth; Cameron C Germe; Nilay Hazari; Brandon Q Mercado; Mycah R Uehling; Susan L Zultanski
Journal:  J Am Chem Soc       Date:  2021-11-30       Impact factor: 15.419

4.  In-Situ Bromination Enables Formal Cross-Electrophile Coupling of Alcohols with Aryl and Alkenyl Halides.

Authors:  Benjamin K Chi; Jonas K Widness; Michael M Gilbert; Daniel C Salgueiro; Kevin J Garcia; Daniel J Weix
Journal:  ACS Catal       Date:  2021-12-21       Impact factor: 13.084

Review 5.  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

6.  Redox-Switchable Behavior of Transition-Metal Complexes Supported by Amino-Decorated N-Heterocyclic Carbenes.

Authors:  Mirko Ruamps; Stéphanie Bastin; Lionel Rechignat; Alix Sournia-Saquet; Laure Vendier; Noël Lugan; Jean-Marie Mouesca; Dmitry A Valyaev; Vincent Maurel; Vincent César
Journal:  Molecules       Date:  2022-06-11       Impact factor: 4.927

7.  Potent Reductants via Electron-Primed Photoredox Catalysis: Unlocking Aryl Chlorides for Radical Coupling.

Authors:  Nicholas G W Cowper; Colleen P Chernowsky; Oliver P Williams; Zachary K Wickens
Journal:  J Am Chem Soc       Date:  2020-01-17       Impact factor: 15.419

8.  Electrochemical Activation of Diverse Conventional Photoredox Catalysts Induces Potent Photoreductant Activity*.

Authors:  Colleen P Chernowsky; Alyah F Chmiel; Zachary K Wickens
Journal:  Angew Chem Int Ed Engl       Date:  2021-08-23       Impact factor: 16.823

9.  Critical Assessment of the Reducing Ability of Breslow-type Derivatives and Implications for Carbene-Catalyzed Radical Reactions*.

Authors:  Ludivine Delfau; Samantha Nichilo; Florian Molton; Julie Broggi; Eder Tomás-Mendivil; David Martin
Journal:  Angew Chem Int Ed Engl       Date:  2021-11-15       Impact factor: 16.823

10.  Pushing the limits of neutral organic electron donors: a tetra(iminophosphorano)-substituted bispyridinylidene.

Authors:  Samuel S Hanson; Eswararao Doni; Kyle T Traboulsee; Graeme Coulthard; John A Murphy; C Adam Dyker
Journal:  Angew Chem Int Ed Engl       Date:  2015-07-24       Impact factor: 15.336

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