Literature DB >> 19229586

Recent synthesis of aminophosphonic acids as potential biological importance.

Emilia D Naydenova1, Petar T Todorov, Kolio D Troev.   

Abstract

Aminophosphonic acids are an important group of medicinal compounds, and their synthesis has been a focus of considerable attention in synthetic organic chemistry as well as medicinal chemistry. Although the phosphonic and carboxylic acid groups differ considerably with respect to shape, size, and acidity, alpha-aminophosphonic acids are considered to be structural analogues of the corresponding amino acids and the transition state mimics peptide hydrolysis. This review summarizes recent developments in the synthesis, characterization and biological activity of alpha-aminophosphonic acid and N-analogues. An account of both uses will be presented, emphasizing one of the potential future developments, and some implications in medicinal chemistry are also disclosed. In addition, a brief account on the characterization of N-(phosphonomethyl) glycine derivatives will be presented.

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Year:  2009        PMID: 19229586     DOI: 10.1007/s00726-009-0254-7

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  16 in total

1.  A Comparative Study of Stabilities and Coordination Modes of β-Alaninephosphonic Acid in Copper(II) Heteroligand Complexes with Ethylenediamine, Diethylenetriamine or N,N,N',N',N″-Pentamethyldiethylene Triamine in Aqueous Solution.

Authors:  Anna Kamecka
Journal:  J Solution Chem       Date:  2012-11-08       Impact factor: 1.677

2.  New approaches towards the synthesis of 1,2,3,4-tetrahydro isoquinoline-3-phosphonic acid (TicP).

Authors:  José Luis Viveros-Ceballos; Lizeth A Matías-Valdez; Francisco J Sayago; Carlos Cativiela; Mario Ordóñez
Journal:  Amino Acids       Date:  2021-03-01       Impact factor: 3.520

3.  Redox-neutral α-C-H bond functionalization of secondary amines with concurrent C-P bond formation/N-alkylation.

Authors:  Deepankar Das; Daniel Seidel
Journal:  Org Lett       Date:  2013-08-19       Impact factor: 6.005

4.  Pyrrolidine and oxazolidine ring transformations in proline and serine derivatives of α-hydroxyphosphonates induced by deoxyfluorinating reagents.

Authors:  Patrycja Kaczmarek; Magdalena Rapp; Henryk Koroniak
Journal:  RSC Adv       Date:  2018-07-06       Impact factor: 4.036

Review 5.  Synthesis of α-Aminophosphonates and Related Derivatives; the Last Decade of the Kabachnik-Fields Reaction.

Authors:  Petra R Varga; György Keglevich
Journal:  Molecules       Date:  2021-04-25       Impact factor: 4.411

6.  Synthesis, cytotoxicity, DNA binding and apoptosis of rhein-phosphonate derivatives as antitumor agents.

Authors:  Man-Yi Ye; Gui-Yang Yao; Jing-Chen Wei; Ying-Ming Pan; Zhi-Xin Liao; Heng-Shan Wang
Journal:  Int J Mol Sci       Date:  2013-04-29       Impact factor: 5.923

7.  (R)-Methyl {[(2-carb-oxy-bicyclo-[2.2.2]octan-1-yl)-ammonio]-methyl}-phos-phon-ate dichloro-methane 0.25-solvate.

Authors:  Petar Todorov; Monique Calmes; Boris L Shivachev; Rosica P Nikolova
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-07-30

8.  Fungal platform for direct chiral phosphonic building blocks production. Closer look on conversion pathway.

Authors:  Ewa Żymańczyk-Duda; Małgorzata Brzezińska-Rodak; Kinga Kozyra; Magdalena Klimek-Ochab
Journal:  Appl Biochem Biotechnol       Date:  2014-11-16       Impact factor: 2.926

9.  Highly Diastereoselective Construction of Carbon- Heteroatom Quaternary Stereogenic Centers in the Synthesis of Analogs of Bioactive Compounds: From Monofluorinated Epoxyalkylphosphonates to α-Fluoro-, β-, or γ-Amino Alcohol Derivatives of Alkylphosphonates.

Authors:  Magdalena Rapp; Klaudia Margas-Musielak; Patrycja Kaczmarek; Agnieszka Witkowska; Tomasz Cytlak; Tomasz Siodła; Henryk Koroniak
Journal:  Front Chem       Date:  2021-06-02       Impact factor: 5.221

10.  Chiral phosphinate degradation by the fusarium species: scope and limitation of the process.

Authors:  Natalia Kmiecik; Magdalena Klimek-Ochab; Małgorzata Brzezińska-Rodak; Paulina Majewska; Ewa Zymańczyk-Duda
Journal:  Biotechnol Res Int       Date:  2013-11-10
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