Supporting Information
Supporting Information File 1: Detailed experimental procedures, NMR and mass spectra of all compounds. | ||
Format: PDF | Size: 1.9 MB | Download |
Cite the Following Article
Synthesis of acylhydrazino-peptomers, a new class of peptidomimetics, by consecutive Ugi and hydrazino-Ugi reactions
Angélica de Fátima S. Barreto, Veronica Alves dos Santos and Carlos Kleber Z. Andrade
Beilstein J. Org. Chem. 2016, 12, 2865–2872.
https://doi.org/10.3762/bjoc.12.285
How to Cite
Barreto, A. d. F. S.; Santos, V. A. d.; Andrade, C. K. Z. Beilstein J. Org. Chem. 2016, 12, 2865–2872. doi:10.3762/bjoc.12.285
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
Picture with graphical abstract, title and authors for social media postings and presentations. | ||
Format: PNG | Size: 233.4 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Juszczak, K.; Szczepankiewicz, W.; Walczak, K. Synthesis and Primary Activity Assay of Novel Benitrobenrazide and Benserazide Derivatives. Molecules (Basel, Switzerland) 2024, 29, 629. doi:10.3390/molecules29030629
- Hooshmand, S. E.; Zhang, W. Ugi Four-Component Reactions Using Alternative Reactants. Molecules (Basel, Switzerland) 2023, 28, 1642. doi:10.3390/molecules28041642
- Anugu, N.; Thunga, S.; Poshala, S.; Kokatla, H. P. N-Oxide-Induced Ugi Reaction: A Rapid Access to Quinoline-C2-amino Amides via Deoxygenative C(sp2)-H Functionalization. The Journal of organic chemistry 2022, 87, 10435–10440. doi:10.1021/acs.joc.2c00904
- Zhu, Y.; Tao, Y. Sequence-controlled and sequence-defined polypeptoids via the Ugi reaction: synthesis and sequence-driven properties. Polymer Chemistry 2021, 12, 4895–4902. doi:10.1039/d1py00658d
- Agouram, N.; Hadrami, E. M. E.; Bentama, A. 1,2,3-Triazoles as Biomimetics in Peptide Science. Molecules (Basel, Switzerland) 2021, 26, 2937. doi:10.3390/molecules26102937
- Fouad, M. A.; Abdel-Hamid, H.; Ayoup, M. S. Two decades of recent advances of Ugi reactions: synthetic and pharmaceutical applications. RSC advances 2020, 10, 42644–42681. doi:10.1039/d0ra07501a
- Samarasimhareddy, M.; Shamir, M.; Shalev, D. E.; Hurevich, M.; Friedler, A. A Rapid and Efficient Building Block Approach for Click Cyclization of Peptoids. Frontiers in chemistry 2020, 8, 405. doi:10.3389/fchem.2020.00405
- de Fátima S. Barreto, A.; Andrade, C. K. Z. Microwave-mediated synthesis of a cyclic heptapeptoid through consecutive Ugi reactions. Tetrahedron 2018, 74, 6861–6865. doi:10.1016/j.tet.2018.10.018
- Pilli, R. A.; de Assis, F. F. Organic Synthesis: New Vistas in the Brazilian Landscape. Anais da Academia Brasileira de Ciencias 2018, 90, 895–941. doi:10.1590/0001-3765201820170564
- de Fátima S. Barreto, A.; dos Santos, V. A.; Andrade, C. K. Z. Consecutive hydrazino-Ugi-azide reactions: synthesis of acylhydrazines bearing 1,5-disubstituted tetrazoles. Beilstein journal of organic chemistry 2017, 13, 2596–2602. doi:10.3762/bjoc.13.256