Results 111 to 120 of about 2,043,921 (203)
Conjugation of oligonucleotides with activated carbamate reagents prepared by the Ugi reaction for oligonucleotide library synthesis. [PDF]
Kita R, Osawa T, Obika S.
europepmc +1 more source
Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi reaction/catalyst-free intramolecular azide-alkyne cycloaddition. [PDF]
Mazur MO +8 more
europepmc +1 more source
The well-known aminoazoles, 3-amino-5-methylisoxazole and 5-amino-N-aryl-1H-pyrazole-4-carboxamides, were studied as an amine component in Ugi and Groebke–Blackburn–Bienaymé multicomponent reactions.
Maryna V. Murlykina +8 more
doaj +1 more source
Tritylamine as an Ammonia Surrogate in the Ugi Reaction Provides Access to Unprecedented 5-Sulfamido Oxazoles Using Burgess-type Reagents. [PDF]
Bhela IP +4 more
europepmc +1 more source
Silver(I) triflate-catalyzed post-Ugi synthesis of pyrazolodiazepines
A silver(I) triflate-catalyzed post-Ugi assembly of novel pyrazolo[1,5-a][1,4]diazepine scaffolds is reported offering high yields (up to 98%) under mild conditions.
Muhammad Hasan +6 more
doaj +1 more source
Ugi reaction in the synthesis of Janus dendrimers as nanocarriers of chlorambucil and ibuprofen
The synthesis and characterization of Janus dendrimers conjugated with two drugs: chlorambucil and ibuprofen are reported. The dendrons by the Ugi reaction were obtained.
Israel Barajas-Mendoza +2 more
doaj +1 more source
A solid-phase approach including on-resin Ugi reactions was developed for the construction of β-hairpins. Various N-alkylated dipeptide fragments proved capable of aligning antiparallel β-sheets in a macrocyclic scaffold, thus serving as β-hairpin ...
Ludger A. Wessjohann +7 more
core +1 more source
The three-component Ugi reaction with chiral 2-(2-formyl-1H-pyrrol-1-yl)acetic acids prepared from natural l-aminoacids was investigated. The reaction opens a new route to chiral substituted pyrroloketopiperazines.
Reznichenko, Alexander L.; id_orcid +5 more
core +1 more source
Here we report an organocatalytic double Ugi reaction combining the enantioselective process and ee enhancement in a single operation to afford the chiral Ugi products with very high ee values.
Tong, Shuo +3 more
core +1 more source

