Literature DB >> 19827067

Oxidative halogenation with "green" oxidants: oxygen and hydrogen peroxide.

Ajda Podgorsek1, Marko Zupan, Jernej Iskra.   

Abstract

It is difficult to imagine organic chemistry without organo-halogen compounds and the molecular halogens needed for their preparation. The halogens have very different reactivity, with iodine usually requiring some form of activation, while others are reactive and hazardous chemicals. To avoid their use, various modified reagents have been discovered (N-bromo- and N-chlorosuccinimide, Selectfluor..), but halogens are used to prepare these reagents and when they are used the atom economy is poor. A better approach, which is based on biomimetric research on oxidative halogenation in nature, consists of generating the halogenating reagent in situ under acidic conditions from a halide salt. The result of such a reaction has been halogenation with 100 % halogen atom economy. Suitable oxidants for the oxidation of halides are hydrogen peroxide and oxygen.

Entities:  

Year:  2009        PMID: 19827067     DOI: 10.1002/anie.200901223

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


  29 in total

1.  Improving the stability and catalyst lifetime of the halogenase RebH by directed evolution.

Authors:  Catherine B Poor; Mary C Andorfer; Jared C Lewis
Journal:  Chembiochem       Date:  2014-05-21       Impact factor: 3.164

2.  Abiotic Bromination of Soil Organic Matter.

Authors:  Alessandra C Leri; Bruce Ravel
Journal:  Environ Sci Technol       Date:  2015-10-27       Impact factor: 9.028

3.  Enantioselective Desymmetrization of Methylenedianilines via Enzyme-Catalyzed Remote Halogenation.

Authors:  James T Payne; Paul H Butkovich; Yifan Gu; Kyle N Kunze; Hyun June Park; Duo-Sheng Wang; Jared C Lewis
Journal:  J Am Chem Soc       Date:  2018-01-08       Impact factor: 15.419

4.  Aromatic Halogenation by Using Bifunctional Flavin Reductase-Halogenase Fusion Enzymes.

Authors:  Mary C Andorfer; Ketaki D Belsare; Anna M Girlich; Jared C Lewis
Journal:  Chembiochem       Date:  2017-09-22       Impact factor: 3.164

5.  Synthesis, Anticancer Potential and Comprehensive Toxicity Studies of Novel Brominated Derivatives of Bacterial Biopigment Prodigiosin from Serratia marcescens ATCC 27117.

Authors:  Jelena Lazic; Sanja Skaro Bogojevic; Sandra Vojnovic; Ivana Aleksic; Dusan Milivojevic; Martin Kretzschmar; Tanja Gulder; Milos Petkovic; Jasmina Nikodinovic-Runic
Journal:  Molecules       Date:  2022-06-09       Impact factor: 4.927

6.  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

7.  Regioselective arene halogenation using the FAD-dependent halogenase RebH.

Authors:  James T Payne; Mary C Andorfer; Jared C Lewis
Journal:  Angew Chem Int Ed Engl       Date:  2013-04-16       Impact factor: 15.336

Review 8.  Understanding and Improving the Activity of Flavin-Dependent Halogenases via Random and Targeted Mutagenesis.

Authors:  Mary C Andorfer; Jared C Lewis
Journal:  Annu Rev Biochem       Date:  2018-03-28       Impact factor: 23.643

9.  Regioselectivity of substrate hydroxylation versus halogenation by a nonheme iron(IV)-oxo complex: possibility of rearrangement pathways.

Authors:  Matthew G Quesne; Sam P de Visser
Journal:  J Biol Inorg Chem       Date:  2012-05-13       Impact factor: 3.358

10.  Flavin-dependent halogenases catalyze enantioselective olefin halocyclization.

Authors:  Dibyendu Mondal; Brian F Fisher; Yuhua Jiang; Jared C Lewis
Journal:  Nat Commun       Date:  2021-06-01       Impact factor: 14.919

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