Abstract
An effective procedure for the synthesis of long-chain alkyl esters of aminoacids is described. The procedure was studied for the practical synthesis of methionine nonylate, using tosyl chloride to generate in situ intermediate tosylates of aminoacids.
Keywords: Fatty alcohol, amino acids, esterification, p-tosyl chloride.
Letters in Organic Chemistry
Title:A Study of Aminoacid Esterification with Nonanol
Volume: 10 Issue: 6
Author(s): Cristian Simion, Alina Culetu and Alina Marieta Simion
Affiliation:
Keywords: Fatty alcohol, amino acids, esterification, p-tosyl chloride.
Abstract: An effective procedure for the synthesis of long-chain alkyl esters of aminoacids is described. The procedure was studied for the practical synthesis of methionine nonylate, using tosyl chloride to generate in situ intermediate tosylates of aminoacids.
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Cite this article as:
Simion Cristian, Culetu Alina and Simion Marieta Alina, A Study of Aminoacid Esterification with Nonanol, Letters in Organic Chemistry 2013; 10 (6) . https://dx.doi.org/10.2174/15701786113109990005
DOI https://dx.doi.org/10.2174/15701786113109990005 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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