Literature DB >> 24022085

Facile and efficient KOH-catalysed reduction of esters and tertiary amides.

José A Fernández-Salas1, Simone Manzini, Steven P Nolan.   

Abstract

Esters and tertiary amides were efficiently reduced to their corresponding alcohols and amines in high yields under mild and environmentally friendly conditions. The presented KOH-catalysed system involves a simple hydrosilylation procedure that is carried out under solvent-free conditions and does not require the use of inert conditions.

Entities:  

Year:  2013        PMID: 24022085     DOI: 10.1039/c3cc45930f

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


  4 in total

1.  From a decomposition product to an efficient and versatile catalyst: the [Ru(η5-indenyl)(PPh3)2Cl] story.

Authors:  Simone Manzini; José A Fernández-Salas; Steven P Nolan
Journal:  Acc Chem Res       Date:  2014-09-29       Impact factor: 22.384

2.  Phenylsilane as an effective desulfinylation reagent.

Authors:  Wanda H Midura; Aneta Rzewnicka; Jerzy A Krysiak
Journal:  Beilstein J Org Chem       Date:  2017-08-01       Impact factor: 2.883

3.  Early Main Group Metal Catalysts for Imine Hydrosilylation.

Authors:  Holger Elsen; Christian Fischer; Christian Knüpfer; Ana Escalona; Sjoerd Harder
Journal:  Chemistry       Date:  2019-10-16       Impact factor: 5.236

4.  An efficient and atom-economical route to N-aryl amino alcohols from primary amines.

Authors:  Zhen Xiao; Juanjuan Li; Qiang Yue; Qian Zhang; Dong Li
Journal:  RSC Adv       Date:  2018-10-05       Impact factor: 3.361

  4 in total

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