Abstract
Threonine-proline chimeras are not so abundant in nature as the other proine-chimeras and their functionalization is also restricted to the third position on the pyrrolidine ring. Despite these aspects the synthetic procedures adopted to obtain these products are straightforward and well-described in literature, as reported in the following review.
Keywords: Threonine-proline chimeras, diastereoselective cyclization, Sharpless epoxidation, Deckmann reaction, Michael condensation.
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Current Bioactive Compounds
Title:Threonine-Proline-Chimeras, A Valuable Building Block for Peptidomimetic Design: A Review
Volume: 12 Issue: 3
Author(s): Adriano Mollica and Gokhan Zengin
Affiliation:
Keywords: Threonine-proline chimeras, diastereoselective cyclization, Sharpless epoxidation, Deckmann reaction, Michael condensation.
Abstract: Threonine-proline chimeras are not so abundant in nature as the other proine-chimeras and their functionalization is also restricted to the third position on the pyrrolidine ring. Despite these aspects the synthetic procedures adopted to obtain these products are straightforward and well-described in literature, as reported in the following review.
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Cite this article as:
Mollica Adriano and Zengin Gokhan, Threonine-Proline-Chimeras, A Valuable Building Block for Peptidomimetic Design: A Review, Current Bioactive Compounds 2016; 12 (3) . https://dx.doi.org/10.2174/1573407212666160511162638
DOI https://dx.doi.org/10.2174/1573407212666160511162638 |
Print ISSN 1573-4072 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6646 |
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