Issue 1, 2006
From the journal:

Green Chemistry

Benign approaches for the synthesis of bis-imine Schiff bases

Tania R. van den Ancker,*a   Gareth W. V. Caveb  and  Colin L. Rastonc  

* Corresponding authors

a Department of Biological and Physical Sciences, University of Southern Queensland, Toowoomba, Australia
E-mail: ancker@usq.edu.au
Fax: +61 7 4631 1530
Tel: +61 7 4631 2363

b School of Biomedical and Natural Sciences, Nottingham Trent University, Nottingham, UK
E-mail: gareth.cave@ntu.ac.uk
Fax: +44 (0)115 848 6636
Tel: +44 (0)115 848 3242

c School of Biomedical, Biomolecular and Chemical Sciences, University of Western Australia, Crawley, Australia
E-mail: clraston@chem.uwa.edu.au
Fax: +61 8 9380 1005
Tel: +61 8 9380 3045

Abstract

Pure bis-imine Schiff bases are readily accessible in high yield, typically >95%, when aliphatic diamine/aldehyde condensation reactions are carried out under solvent-free conditions or in poly(propyleneglycol) (PPG) as a recyclable reaction medium, with negligible waste.

Graphical abstract: Benign approaches for the synthesis of bis-imine Schiff bases

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Article information

DOI
https://doi.org/10.1039/B513289D
Article type
Paper
Submitted
22 Sep 2005
Accepted
28 Oct 2005
First published
17 Nov 2005

Green Chem., 2006,8, 50-53

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Benign approaches for the synthesis of bis-imine Schiff bases

T. R. van den Ancker, G. W. V. Cave and C. L. Raston, Green Chem., 2006, 8, 50 DOI: 10.1039/B513289D

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