Results 121 to 130 of about 2,155,266 (206)

One-pot synthesis of oxoisoindoline-1,2,3-triazole hybrid by a Ugi–click reaction

open access: yes, 2016
1,2,3-Triazole-3-oxoisoindoline-1-carboxamide system was successfully synthesized by using a combination of Ugi and click reactions. This two-step, one-pot synthesis was started by the reaction of 2-formyl benzoic acid, propargyl amine, and cyclohexyl ...
Loghman Firoozpour (657961)   +6 more
core   +1 more source

Synthesis of novel 1,4 naphthoquinone-based molecules by an Ugi-type four-component reaction

open access: yes, 2019
In an attempt to further exploit multicomponent reactions in the field of 1,4 naphthoquinone-based compounds, we describe an Ugi-type multicomponent approach for the synthesis of novel 3-substituted 1,4 naphthoquinone molecules. The process relies on the
Waléria F. Rabêlo (6381617)   +1 more
core   +1 more source

The First Example of a Diastereoselective Thio-Ugi Reaction:  A New Synthetic Approach to Chiral Imidazole Derivatives

open access: yes, 2016
The first example of a diastereoselective thio-Ugi reaction with chiral α-methylbenzylamine is described. The reaction results in formation of two diastereomers of thioamides, the major of which was isolated.
Valentine G. Nenajdenko (1519807)   +2 more
core   +1 more source

Revisited Mechanistic Implications of the Joullié–Ugi Three-Component Reaction

open access: yes, 2016
The effect of the solvent on the diastereoselectivity of the Joullié–Ugi three-component reaction (JU-3CR) using an α-substituted five-membered cyclic imine is revisited.
Akira Matsuda (9292)   +2 more
core   +1 more source

Electrochemical TEMPO-Catalyzed Oxidative Ugi-Type Reaction

open access: yesACS Organic & Inorganic Au, 2021
Na Pan   +4 more
doaj   +1 more source

Exploration of a Tandem Diels-Alder Ugi-Smiles Reaction

open access: yes, 2014
A multicomponent coupling reaction (MCR) is a very efficient synthetic method, capable of forming several new bonds in a one-pot process to afford highly functionalized molecules.
Richey, Bree
core  

Access to Cyclic Monensin Derivatives via a Four-Component Ugi Reaction. [PDF]

open access: yesJ Org Chem
Graniczny R   +5 more
europepmc   +1 more source

Halogenated Reagents in the Ugi Reaction: From Rearrangement Reactions to Ketal Synthesis. [PDF]

open access: yesACS Omega
González-Saiz B   +5 more
europepmc   +1 more source

Synthesis of ionizable lipopolymers using split-Ugi reaction for pulmonary delivery of various size RNAs and gene editing. [PDF]

open access: yesNat Commun
Vlasova KY   +12 more
europepmc   +1 more source

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