Literature DB >> 25001487

Efficient metal-free hydrosilylation of tertiary, secondary and primary amides to amines.

Enguerrand Blondiaux1, Thibault Cantat.   

Abstract

Hydrosilylation of secondary and tertiary amides to amines is described using catalytic amounts of B(C6F5)3. The organic catalyst enables the reduction of amides with cost-efficient, non-toxic and air stable PMHS and TMDS hydrosilanes. The methodology was successfully extended to the more challenging reduction of primary amides.

Entities:  

Year:  2014        PMID: 25001487     DOI: 10.1039/c4cc02894e

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


  5 in total

1.  Site Selective Amide Reduction of Cyclosporine A Enables Diverse Derivation of an Important Cyclic Peptide.

Authors:  Michael T Peruzzi; Fabrice Gallou; Stephen J Lee; Michel R Gagné
Journal:  Org Lett       Date:  2019-04-17       Impact factor: 6.005

2.  Efficient and selective hydrogenation of amides to alcohols and amines using a well-defined manganese-PNN pincer complex.

Authors:  Veronica Papa; Jose R Cabrero-Antonino; Elisabetta Alberico; Anke Spanneberg; Kathrin Junge; Henrik Junge; Matthias Beller
Journal:  Chem Sci       Date:  2017-03-08       Impact factor: 9.825

Review 3.  Tris(pentafluorophenyl)borane-Catalyzed Reactions Using Silanes.

Authors:  Taylor Hackel; Nicholas A McGrath
Journal:  Molecules       Date:  2019-01-25       Impact factor: 4.411

Review 4.  Defunctionalisation catalysed by boron Lewis acids.

Authors:  Huaquan Fang; Martin Oestreich
Journal:  Chem Sci       Date:  2020-07-28       Impact factor: 9.825

5.  Towards a general ruthenium-catalyzed hydrogenation of secondary and tertiary amides to amines.

Authors:  Jose R Cabrero-Antonino; Elisabetta Alberico; Kathrin Junge; Henrik Junge; Matthias Beller
Journal:  Chem Sci       Date:  2016-02-09       Impact factor: 9.825

  5 in total

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