Abstract
Chemical strategies developed for the solid-phase synthesis of hydroxamates are divided into four groups: (i) the traditional synthesis of hydroxamates via cleavage of resin-bound esters by hydroxylamine and its derivatives, (ii) introduction of hydroxamic acid moiety on the resin-bound precursor, (iii) transformation of polymer-supported hydroxylamine, attached to a solid supported linker either by oxygen (O-linking strategy) or by nitrogen (N-linking strategy), and (iv) synthesis of N-alkyl hydroxamates. The scope and limitation of individual approaches are discussed.
Keywords: Hydroxamic acid, hydroxamate, solid-phase synthesis
Mini-Reviews in Medicinal Chemistry
Title: Solid-Phase Synthesis of Biologically Interesting Compounds Containing Hydroxamic Acid Moiety
Volume: 6 Issue: 1
Author(s): Viktor Krchnak
Affiliation:
Keywords: Hydroxamic acid, hydroxamate, solid-phase synthesis
Abstract: Chemical strategies developed for the solid-phase synthesis of hydroxamates are divided into four groups: (i) the traditional synthesis of hydroxamates via cleavage of resin-bound esters by hydroxylamine and its derivatives, (ii) introduction of hydroxamic acid moiety on the resin-bound precursor, (iii) transformation of polymer-supported hydroxylamine, attached to a solid supported linker either by oxygen (O-linking strategy) or by nitrogen (N-linking strategy), and (iv) synthesis of N-alkyl hydroxamates. The scope and limitation of individual approaches are discussed.
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Cite this article as:
Krchnak Viktor, Solid-Phase Synthesis of Biologically Interesting Compounds Containing Hydroxamic Acid Moiety, Mini-Reviews in Medicinal Chemistry 2006; 6 (1) . https://dx.doi.org/10.2174/138955706775197811
DOI https://dx.doi.org/10.2174/138955706775197811 |
Print ISSN 1389-5575 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5607 |
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