Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/36372
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Type: Journal article
Title: An amino acid N-derivatising group that can be coloured on demand
Author: Abell, A.
Martyn, D.
May, B.
Nabbs, B.
Citation: Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 2002; 43(20):3673-3675
Publisher: Pergamon-Elsevier Science Ltd
Issue Date: 2002
ISSN: 0040-4039
Statement of
Responsibility: 
Andrew D. Abell, Derek C. Martyn, Barnaby C. H. May and Brent K. Nabbs
Abstract: A method is presented whereby an amino acid is reacted with 5-formyl-1H-pyrrole-2-carboxylic acid to give an N-derivatised tag that has a latent ability to be coloured. A characteristic red pyrrolizin-3-one (coloured tag) is then revealed on treatment with hydrocinnamoyl chloride. This sequence has been carried out on amino acids in solution, and on solid phase, and also on dipeptides. A method is presented whereby an amino acid is reacted with 5-formyl-1H-pyrrole-2-carboxylic acid to give an N-derivatised tag that has a latent ability to be coloured.
DOI: 10.1016/S0040-4039(02)00625-1
Description (link): http://www.sciencedirect.com/science/journal/00404039
Published version: http://dx.doi.org/10.1016/s0040-4039(02)00625-1
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Chemistry publications

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