Literature DB >> 22307077

A general and selective copper-catalyzed reduction of secondary amides.

Shoubhik Das1, Benoît Join, Kathrin Junge, Matthias Beller.   

Abstract

In situ-generated cationic copper/pybox catalyst systems allow for the selective reduction of secondary amides into the corresponding amines under mild conditions. This novel protocol has a wide substrate scope and shows good functional group tolerance. This journal is © The Royal Society of Chemistry 2012

Entities:  

Year:  2012        PMID： 22307077     DOI： 10.1039/c2cc17209g

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


  4 in total

1.  Nickel-Catalyzed Reduction of Secondary and Tertiary Amides.

Authors:  Bryan J Simmons; Marie Hoffmann; Jaeyeon Hwang; Moritz K Jackl; Neil K Garg
Journal:  Org Lett       Date:  2017-03-24       Impact factor: 6.005

2.  Metal- and solvent-free synthesis of amides using substitute formamides as an amino source under mild conditions.

Authors:  Feng Zhang; Lesong Li; Jingyu Zhang; Hang Gong
Journal:  Sci Rep       Date:  2019-02-26       Impact factor: 4.379

3.  Hydrocarbon Synthesis via Photoenzymatic Decarboxylation of Carboxylic Acids.

Authors:  Wuyuan Zhang; Ming Ma; Mieke M E Huijbers; Georgy A Filonenko; Evgeny A Pidko; Morten van Schie; Sabrina de Boer; Bastien O Burek; Jonathan Z Bloh; Willem J H van Berkel; Wilson A Smith; Frank Hollmann
Journal:  J Am Chem Soc       Date:  2019-02-06       Impact factor: 15.419

4.  Highly chemoselective reduction of amides (primary, secondary, tertiary) to alcohols using SmI2/amine/H2O under mild conditions.

Authors:  Michal Szostak; Malcolm Spain; Andrew J Eberhart; David J Procter
Journal:  J Am Chem Soc       Date:  2014-01-31       Impact factor: 15.419
  4 in total

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