Literature DB >> 11405674

In situ oxidation-imine formation-reduction routes from alcohols to amines.

L Blackburn1, R J Taylor.   

Abstract

Manganese dioxide is employed as an in situ oxidant for the one-pot conversion of alcohols into imines. In combination with polymer-supported cyanoborohydride (PSCBH), a one-pot oxidation-imine formation-reduction sequence is reported. This procedure enables alcohols to be converted directly into both secondary and tertiary amines.

Entities:  

Year:  2001        PMID： 11405674     DOI： 10.1021/ol015819b

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  A facile approach to 2-alkoxyindolin-3-one and its application to the synthesis of N-benzyl matemone.

Authors:  Makoto Shimizu; Hayao Imazato; Isao Mizota; Yusong Zhu
Journal:  RSC Adv       Date:  2019-06-03       Impact factor: 4.036

2.  Combinatorial synthesis of chemical building blocks 1. Azomethines.

Authors:  Sergey V Ryabukhin; Dmitriy M Panov; Andrey S Plaskon; Alexander Chuprina; Sergey E Pipko; Andrey A Tolmachev; Alexander N Shivanyuk
Journal:  Mol Divers       Date:  2012-10-30       Impact factor: 2.943

3.  Efficient and selective N-alkylation of amines with alcohols catalysed by manganese pincer complexes.

Authors:  Saravanakumar Elangovan; Jacob Neumann; Jean-Baptiste Sortais; Kathrin Junge; Christophe Darcel; Matthias Beller
Journal:  Nat Commun       Date:  2016-10-06       Impact factor: 14.919
  3 in total

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