Abstract
A facile route to synthesize amide type N-9-purinyl-acetic acid derivatives both in guanine and hypoxanthine series is described. The regioselective alkylation of the 6-chloro-purine derivatives followed by their conversion into guanine or hypoxanthine nucleus in mild acidic conditions, are the key steps that allow the efficient preparation of compounds with an acetic function coupled with various amino acids.
Keywords: Purinyl-acetic acid derivatives, peptide coupling, hypoxanthine, guanine
Letters in Organic Chemistry
Title: A Simple and High-Yield Route to N-9-purinyl-acetic Acid Derivatives Coupled with Amino Acids
Volume: 5 Issue: 6
Author(s): Marie-Emmanuelle Million, Sylvie Radix, Sebastien Marrot, Magali Imbert and Joelle Paris
Affiliation:
Keywords: Purinyl-acetic acid derivatives, peptide coupling, hypoxanthine, guanine
Abstract: A facile route to synthesize amide type N-9-purinyl-acetic acid derivatives both in guanine and hypoxanthine series is described. The regioselective alkylation of the 6-chloro-purine derivatives followed by their conversion into guanine or hypoxanthine nucleus in mild acidic conditions, are the key steps that allow the efficient preparation of compounds with an acetic function coupled with various amino acids.
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Cite this article as:
Million Marie-Emmanuelle, Radix Sylvie, Marrot Sebastien, Imbert Magali and Paris Joelle, A Simple and High-Yield Route to N-9-purinyl-acetic Acid Derivatives Coupled with Amino Acids, Letters in Organic Chemistry 2008; 5(6) . https://dx.doi.org/10.2174/157017808785740408
DOI https://dx.doi.org/10.2174/157017808785740408 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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