Cargando…
Synthesis of imidazo[1,2-a]pyridine-containing peptidomimetics by tandem of Groebke–Blackburn–Bienaymé and Ugi reactions
Peptidomimetics with a substituted imidazo[1,2-a]pyridine fragment were synthesized by a tandem of Groebke–Blackburn–Bienaymé and Ugi reactions. The target products contain substituted imidazo[1,2-a]pyridine and peptidomimetic moieties as pharmacophores with four diversity points introduced from rea...
Autores principales: | Kolomiiets, Oleksandr V, Tsygankov, Alexander V, Kornet, Maryna N, Brazhko, Aleksander A, Musatov, Vladimir I, Chebanov, Valentyn A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241102/ https://www.ncbi.nlm.nih.gov/pubmed/37284590 http://dx.doi.org/10.3762/bjoc.19.53 |
Ejemplares similares
-
Novel 5-Nitrofuran-Tagged Imidazo-Fused Azines and Azoles Amenable by the Groebke–Blackburn–Bienaymé Multicomponent Reaction: Activity Profile against ESKAPE Pathogens and Mycobacteria
por: Sapegin, Alexander, et al.
Publicado: (2022) -
Doebner-type pyrazolopyridine carboxylic acids in an Ugi four-component reaction
por: Murlykina, Maryna V, et al.
Publicado: (2019) -
Diversity‐Oriented Synthesis of [2.2]Paracyclophane‐derived Fused Imidazo[1,2‐a]heterocycles by Groebke‐Blackburn‐Bienaymé Reaction: Accessing Cyclophanyl Imidazole Ligands Library
por: Stahlberger, Mareen, et al.
Publicado: (2021) -
Solvent- and Catalyst-Free One-Pot Green Bound-Type
Fused Bis-Heterocycles Synthesis via Groebke–Blackburn–Bienaymé
Reaction/S(N)Ar/Ring-Chain Azido-Tautomerization Strategy
por: Claudio-Catalán, Miguel Ángel, et al.
Publicado: (2018) -
New tricks of well-known aminoazoles in isocyanide-based multicomponent reactions and antibacterial activity of the compounds synthesized
por: Murlykina, Maryna V, et al.
Publicado: (2017)