Literature DB >> 25346336

"Nanorust"-catalyzed benign oxidation of amines for selective synthesis of nitriles.

Rajenahally V Jagadeesh1, Henrik Junge, Matthias Beller.   

Abstract

Organic nitriles constitute key precursors and central intermediates in organic synthesis. In addition, nitriles represent a versatile motif found in numerous medicinally and biologically important compounds. Generally, these nitriles are synthesized by traditional cyanation procedures using toxic cyanides. Herein, we report the selective and environmentally benign oxidative conversion of primary amines for the synthesis of structurally diverse aromatic, aliphatic and heterocyclic nitriles using a reusable "nanorust" (nanoscale Fe2 O3 )-based catalysts applying molecular oxygen.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amines; catalysis; iron; nitriles; oxidations

Mesh:

Substances:

Year:  2014        PMID: 25346336     DOI: 10.1002/cssc.201402613

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  3 in total

1.  Catalytic Aerobic Dehydrogenation of Nitrogen Heterocycles Using Heterogeneous Cobalt Oxide Supported on Nitrogen-Doped Carbon.

Authors:  Andrei V Iosub; Shannon S Stahl
Journal:  Org Lett       Date:  2015-09-02       Impact factor: 6.005

Review 2.  Recent Advances in Carbon-Based Iron Catalysts for Organic Synthesis.

Authors:  Fei Wang; Fuying Zhu; Enxiang Ren; Guofu Zhu; Guo-Ping Lu; Yamei Lin
Journal:  Nanomaterials (Basel)       Date:  2022-10-03       Impact factor: 5.719

3.  Synergistic catalysis on Fe-N x sites and Fe nanoparticles for efficient synthesis of quinolines and quinazolinones via oxidative coupling of amines and aldehydes.

Authors:  Zhiming Ma; Tao Song; Youzhu Yuan; Yong Yang
Journal:  Chem Sci       Date:  2019-09-23       Impact factor: 9.825

  3 in total

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