Literature DB >> 30601486

Electrochemical benzylic oxidation of C-H bonds.

Jason A Marko1, Anthony Durgham, Stacey Lowery Bretz, Wei Liu.   

Abstract

Oxidized products have become increasingly valuable as building blocks for a wide variety of different processes and fine chemistry, especially in the benzylic position. We report herein a sustainable protocol for this transformation through C-H functionalization and is performed using electrochemistry as the main power source and tert-butyl hydroperoxide as the radical source for the C-H abstraction. The temperature conditions reported here do not increase above 50 °C and use an aqueous-based medium. A broad substrate scope is explored, along with bioactive molecules, to give comparable and increased product yields when compared to prior reported literature without the use of electrochemistry.

Entities:  

Year:  2019        PMID: 30601486     DOI: 10.1039/c8cc08768g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Mechanistic Studies on the Hexadecafluorophthalocyanine-Iron-Catalyzed Wacker-Type Oxidation of Olefins to Ketones*.

Authors:  Florian Puls; Felix Seewald; Vadim Grinenko; Hans-Henning Klauß; Hans-Joachim Knölker
Journal:  Chemistry       Date:  2021-10-27       Impact factor: 5.020

2.  Synthesis of Benzylic Alcohols by C-H Oxidation.

Authors:  Lalita Tanwar; Jonas Börgel; Tobias Ritter
Journal:  J Am Chem Soc       Date:  2019-11-05       Impact factor: 15.419

Review 3.  13C-NMR Chemical Shifts in 1,3-Benzazoles as a Tautomeric Ratio Criterion.

Authors:  Efrén V García-Báez; Itzia I Padilla-Martínez; Alejandro Cruz; Martha C Rosales-Hernández
Journal:  Molecules       Date:  2022-09-23       Impact factor: 4.927

  3 in total

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