A study of the cis–trans isomerization preference of N-alkylated peptides containing phosphorus in the side chain and backbone-Reference-Cited by-同舟云学术

A study of the cis–trans isomerization preference of N-alkylated peptides containing phosphorus in the side chain and backbone

Published:2019 Issue:32 Volume:43 Page:12804-12813
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

de la Torre Alexander F.¹²³⁴⁵^ORCID,Ali Akbar⁶⁷⁸^ORCID,Concepcion Odette¹²³⁴⁵^ORCID,Montero-Alejo Ana L.⁹¹⁰¹¹¹²⁵^ORCID,Muñiz Francisco M.¹²³⁴⁵^ORCID,Jiménez Claudio A.¹²³⁴⁵^ORCID,Belmar Julio¹²³⁴⁵^ORCID,Velázquez-Libera José Luis¹³¹⁴¹⁵⁵^ORCID,Hernández-Rodríguez Erix W.¹⁶¹⁷¹⁸¹⁹⁵^ORCID,Caballero Julio¹³¹⁴¹⁵⁵^ORCID

Affiliation:

1. Departamento de Química Orgánica

2. Facultad de Ciencias Químicas

3. Universidad de Concepción

4. Concepción

5. Chile

6. Department of Chemistry

7. University of Sargodha

8. Pakistan

9. Departamento de Física

10. FCNMM

11. Universidad Tecnológica Metropolitana

12. Santiago

13. Centro de Bioinformática y Simulación Molecular (CBSM)

14. Universidad de Talca

15. Talca

16. Escuela de Química y Farmacia

17. Facultad de Medicina

18. Universidad Católica del Maule

19. 3460000 Talca

Abstract

The current work provides a study on the cis–trans isomerization behaviour of N-alkylated peptides decorated with phosphonate ester groups.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

The World Academy of Sciences

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Higher Education Commission, Pakistan

Comisión Nacional de Investigación Científica y Tecnológica

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ02234A

Reference61 articles.

1. Phosphonopeptides, a new class of synthetic antibacterial agents

2. P. Kafarski and B.Lejczak , The biological activity of phosphono– and phosphinopeptides , in Aminophosphonic and Aminophosphinic Acids: Chemistry and Biological Activity , ed. Kukhar V. P. , Hudson H. R. , John Wiley , Chichester , 2000 , ch. 12, pp. 407–442

3. Synthesis and structure-activity relationships of antibacterial phosphonopeptides incorporating (1-aminoethyl)phosphonic acid and (aminomethyl)phosphonic acid

4. Design, Synthesis, and Evaluation of Novel Organophosphorus Inhibitors of Bacterial Ureases

5. Resistance to the Antimicrobial Agent Fosmidomycin and an FR900098 Prodrug through Mutations in the Deoxyxylulose Phosphate Reductoisomerase Gene (dxr)

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ugi efficient synthesis of novel N–alkylated lipopeptides, antimicrobial properties and computational studies in Staphylococcus aureus via MurD antibacterial target;Computational Biology and Chemistry;2023-10

2. Multicomponent synthesis and photophysical study of novel α,β-unsaturated carbonyl depsipeptides and peptoids;Frontiers in Chemistry;2023-08-17

3. Efficient Synthesis of Imine-Carboxylic Acid Functionalized Compounds: Single Crystal, Hirshfeld Surface and Quantum Chemical Exploration;Molecules;2023-03-27

4. One-pot four-component synthesis of novel isothiourea-ethylene-tethered-piperazine derivatives;RSC Advances;2023

5. Strategies to Control the Cis‐Trans Isomerization of Peptoid Amide Bonds;Chemistry – An Asian Journal;2022-04-20